Recall roundup: 25 Jul – 31 Jul 2022
145 official recalls and safety alerts were published in the week of 25 Jul – 31 Jul 2022, down 15% on the week before (171). Most were drugs & medical (57) and vehicles (31); common issues included food allergen (11), fire hazard (8), battery (6). 23 were flagged as serious.
Recalls this week
25 Jul – 31 Jul 2022
By country
By product type
Most recalled brands
Common searches
Most serious
Recalls the agency classed as serious, or with a risk of death, fire, electric shock, drowning or strangulation.
- 2022-07-29
FR
EUBus (BLUEBUS) · 12M IT3
Faulty positioning of the mylar insulating sheet (placed between 2 adjacent cells in the battery) may lead to a short circuit, increasing the risk of fire. The product does not comply with the requirements laid down in…
CYEUChildren's clothing set (EBITA)
The long decorative cords with free ends on the blouse can become trapped during various activities of a child, leading to injuries. The product does not comply with the requirements of the General Product Safety…
DEEUPassenger car (Mercedes-Benz) · GLE-Class
The screw connection of a 12V wiring harness pf the vehicles equipped with plug-in hybrid traction may have been secured with insufficient torque. As a result, the electrical resistance of the connection could increase…
- DEEU
Passenger car (Maserati) · Levante
Improperly attached ground cables of the 48 V motor can lead to electrical faults. As a result, sparks and the smell of burning may occur, which leads to an increased risk of fire. The product does not comply with the…
HUEUUSB charger (SENZHEN) · Bran Design
The insulation of the product is inadequate. The user could receive an electric shock from accessible (live) parts. The product does not comply with the requirements of the Low Voltage Directive nor with the standard…
- 2022-07-28
UKElgetec & Something Cosmetics Ultrapower Ionic Hair Dryer sold via TK Maxx
Risk of electric shock and fire
USGillig, LLC: Battery Pack May Short and Cause Fire
A battery short circuit increases the risk of a fire.
- US
Black Diamond Equipment Recalls PIEPS and Black Diamond Avalanche Transceivers Due to Risk of Loss of Emergency Communications
The recalled transceivers may not switch from SEND mode into SEARCH mode. If this were to occur, the device would not be able to locate a skier in an avalanche, which could result in severe bodily harm or death if the…
- US
Daikin Comfort Technologies Manufacturing (formerly Goodman Manufacturing Company, L.P.) Expands Recall of Evaporator Coil Drain Pans to Include Those Installed with…
The molded plastic drain pan located at the bottom of the evaporator coil can overheat, melt and deform, posing a fire hazard.
CPSCDaikin Comfort Technologies Manufacturing, L.P. (formerly…About 298,300 (In addition, about 44,000 were sold in…Official notice → - US
Ocean Technology Systems Recalls Underwater Communication Devices Due to Fire Hazard
Water can leak into the recalled underwater communication device during a dive and penetrate into the battery pack, causing the battery circuit board to short and ignite after the dive, posing a fire hazard.
CPSCUndersea Systems International Inc., dba Ocean Technology…About 500 (In addition, about 36 were sold in Canada)Official notice →
United States 83
- 2022-07-29
- US
Forest River, Inc.: Awning Fabric May Detach Causing Awning to Drop
An awning that drops or extends beyond normal operation can increase the risk of injury.
- US
VLRV, LLC (Vanleigh RV): Awning Fabric May Detach Causing Awning to Drop
An awning that drops or extends beyond normal operation can increase the risk of injury.
- US
Daimler Trucks North America, LLC: Electrical Short Circuit May Cause Engine Stall
Unexpected engine shut down can increase the risk of a crash.
- US
Daimler Trucks North America, LLC: Electrical Short Circuit May Cause Engine Stall
Unexpected engine shut down can increase the risk of a crash. Additionally, a disabled school bus may require an evacuation procedure in an uncontrolled traffic situation, increasing the risk of injury to passengers.
- US
K.Z., Inc.: Awning Fabric May Detach Causing Awning to Drop
An awning that drops or extends beyond normal operation can increase the risk of injury.
- US
Proterra Operating Company, Inc.: Battery Management System Shutdown
An unexpected battery management system shut down can result in a sudden loss of drive power, increasing the risk of a crash.
- US
Harley-Davidson Motor Company: Turn Signal Indicator Light Malfunction/FMVSS 108
Turn signal indicator lights that fail to alert the operator of a turn signal light failure can increase the risk of a crash.
- 2022-07-28
- US
Eldorado National- California, Inc.: Steering Gear Assembled Incorrectly
A fractured steering gear can cause a loss of steering control, increasing the risk of a crash.
- US
Nissan North America, Inc.: Loss of Power Brake Assist/FMVSS 135
A loss of power brake assist can extend the distance required to stop the vehicle, increasing the risk of a crash.
- US
Gillig, LLC: Battery Pack May Short and Cause Fire
A battery short circuit increases the risk of a fire.
- US
PACCAR Incorporated: Steering Gear Assembled Incorrectly
A fractured steering gear can cause a loss of steering control, increasing the risk of a crash.
- US
International Motors, LLC: Battery Cables Grounded Incorrectly
Excessively hot battery ground cables may cause personal injury during battery maintenance repairs. In addition, a battery post that separates from the battery can result in an engine stall without warning, increasing…
- US
Winnebago Towable: Awning Fabric May Detach Causing Awning to Drop
An awning that drops or extends beyond normal operation can increase the risk of injury.
- US
Chrysler (FCA US, LLC): Damaged Tail Light Side Marker Assembly/FMVSS 108
A tail light side marker that does not illuminate can reduce vehicle visibility to other drivers, increasing the risk of a crash.
- US
Shandong New Continent Tire Co., Ltd.: Tire Sidewall Separation/FMVSS 139
Sidewall separation can lead to tire failure, increasing the risk of a crash.
- US
Cummins, Inc.: Electrical Short Circuit May Cause Engine Stall
An unexpected engine stall can increase the risk of a crash.
- US
Chrysler (FCA US, LLC): Damaged Tail Light Side Marker Assembly/FMVSS 108
A tail light side marker that does not illuminate can reduce vehicle visibility to other drivers, increasing the risk of a crash.
- US
First Choice Glass Baby Bottles Recalled by NUK Due to Violation of the Federal Lead Content Ban; Sold Exclusively on Amazon.com (Recall Alert)
The markings on the outside of the bottles contain levels of lead that exceeds the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
- US
Adventure Sports Recalls Ceramic Pulleys for Cabrinha Switchblade and Drifter Kite Sailing Kites Due to Injury Hazard (Recall Alert)
The ceramic pulleys used in the recalled Switchblade and Drifter kiteboarding kites can cause the bridle line connection to break, which reduces performance in steering and control of the kite, causing the kiteboarder…
- US
Textron Specialized Vehicles Recalls All-Terrain Vehicles (ATVs) Due to Crash Hazard (Recall Alert)
A fuse in the ATV's electrical system can fail during operation, which can result in sudden loss of engine power and headlights, posing a crash hazard.
CPSCTextron Specialized Vehicles, of Augusta, GeorgiaAbout 1,750 (In addition, about 550 were sold in Canada)Official notice → - US
KTM North America Recalls Closed Course Competition Motorcycles Due to Crash and Injury Hazards (Recall Alert)
The motorcycle's connecting rod can break, posing crash and injury hazards.
- US
Black Diamond Equipment Recalls PIEPS and Black Diamond Avalanche Transceivers Due to Risk of Loss of Emergency Communications
The recalled transceivers may not switch from SEND mode into SEARCH mode. If this were to occur, the device would not be able to locate a skier in an avalanche, which could result in severe bodily harm or death if the…
- US
Daikin Comfort Technologies Manufacturing (formerly Goodman Manufacturing Company, L.P.) Expands Recall of Evaporator Coil Drain Pans to Include Those Installed with…
The molded plastic drain pan located at the bottom of the evaporator coil can overheat, melt and deform, posing a fire hazard.
CPSCDaikin Comfort Technologies Manufacturing, L.P. (formerly…About 298,300 (In addition, about 44,000 were sold in…Official notice → - US
Epoch Everlasting Play Recalls Kidoozie Play Tents and Playhouses Due to Flammability Risk and Burn Hazard
The fabric playhouses and play tents fail to meet an industry flammability standard for these products, posing a risk of burn injuries to children.
- US
Ocean Technology Systems Recalls Underwater Communication Devices Due to Fire Hazard
Water can leak into the recalled underwater communication device during a dive and penetrate into the battery pack, causing the battery circuit board to short and ignite after the dive, posing a fire hazard.
CPSCUndersea Systems International Inc., dba Ocean Technology…About 500 (In addition, about 36 were sold in Canada)Official notice → - US
Aesop USA Recalls Bathroom Deodorizing Drops and Oil Burner Blends Due to Failure to Meet Child Resistant Packaging Requirements and Violation of FHSA Labeling…
The recalled products contain low-viscosity hydrocarbons which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant,…
CPSCEmeis Cosmetics Pty Ltd., of Collingwood, Victoria,…About 154,300 (In addition, 21,900 were sold in Canada)Official notice → - 2022-07-27
- US
Volkswagen Group of America, Inc.: Air Bag Inflator May Explode or Deploy Improperly
An inflator explosion may result in sharp metal fragments striking occupants, resulting in serious injury or death. An improper air bag deployment may not properly restrain the occupant, increasing their risk of injury…
- US
Volkswagen Group of America, Inc.: Sunroof Malfunction/FMVSS 118
A sunroof switch that is inadvertently pressed can result in unintended auto-closure of the sunroof, increasing the risk of injury.
- US
BMW of North America, LLC: High Voltage Battery May Short-Circuit
A short-circuit in a high voltage battery increases the risk of a fire.
- US
Corp. Micro Bird, Inc.: Inside Panels Insufficiently Attached/FMVSS 221
Insufficiently attached panels may separate during a crash, increasing the risk of an injury.
- US
Stryker Instruments Div. of Stryker Corporation recalls SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090. Used for counting,…
When scanning sponges out after a surgical procedure, an error may allow for a duplicate sponge to be counted without the prompt to make a case note and allowing the case to close. The software update will prevent the…
FDA · DeviceStryker Instruments Div. of Stryker CorporationThe products were distributed to the following US states: KS and ME.Official notice → - US
LumiraDx recalls LumiraDx SARS-CoV-2 Antibody (Ab) Liquid Quality Control
Modification to the LumiraDx SARS-CoV-2 Antibody (Ab) test that was made outside the scope of the approved EUA.
FDA · DeviceLumiraDxDomestic: AR, CA, FL, MA, MD, NC, NJ, NV, NY, OK, TN, TX, & WI.Official notice → - US
Aesculap Implant Systems LLC recalls Aesculap Sterile disposable fleece drape, Product code: GA414, individually packaged, 50 pieces per shipping unit, product code…
Packaging seal integrity not validated resulting in a lack of sterility assurance.
FDA · DeviceAesculap Implant Systems LLCUnited States: CA, CO, GA, IL, IN, KY, MI, NC, NE, NY, OH, RI, VA and WIOfficial notice → - US
Aesculap Implant Systems LLC recalls AESCULAP S4 Cervical Cross Connector L24mm, S4C CROSS CONNECTOR FIXED 24MM, product code SWT113T. Used in spinal fusion surgery.
Insufficient clamping force of the cross connectors in the spinal surgical system which may lead to movement of the connectors on the rods and/or microparticle abrasion.
FDA · DeviceAesculap Implant Systems LLCUnited States Nationwide distribution in the states of CA, CO, IL, IN, MI, NC,…Official notice → - US
Becton Dickinson & Company recalls BD Connecta Stopcock Without Extension Tube Catalog No. 394601 (OUS)
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination…
FDA · DeviceBecton Dickinson & CompanyWorldwide distribution - US Nationwide distribution in the states of AK, AR,…Official notice → - US
GE Healthcare, LLC recalls SIGNA Premier magnetic resonance scanner, model 5748519.
Under rare conditions, SIGNA Premier gradient coils could result in elevated acoustic noise during scanning. After prolonged periods of elevated acoustic noise, this could potentially lead to hearing loss.
FDA · DeviceGE Healthcare, LLCWorldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice → - US
Aesculap Implant Systems LLC recalls ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R
Fracture or breakage of the spinal fixation arm at the downtube instrument if the 90 degree angle is not met when using the removal key with the spinal fixation system.
FDA · DeviceAesculap Implant Systems LLCUnited States Nationwide distribution in the states of CA, CO, IL, MI, OH & TX.Official notice → - US
GE Healthcare, LLC recalls GE Healthcare Avance CS2, Avance CS2 Pro Anesthesia Systems, Part #1009-9050-000; and Aisys CS2 Anesthesia Systems, Part # 1011-9050-000.
The base of the anesthesia system can have a crack and could potentially fracture resulting in a tip or overbalance of the anesthesia system. This can result in potential injury if it falls on a person.
FDA · DeviceGE Healthcare, LLCDistribution was made to AZ, CA, CO, CT, FL, IA, ID, IL, IN, KY, LA, MA, MD,…Official notice → - US
Siemens Medical Solutions USA, Inc recalls Sensis with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or…
Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period of inactivity to the Sensis Vibe system resulting…
FDA · DeviceSiemens Medical Solutions USA, IncUS Nationwide Distribution AZ FL KY MI OH PR TXOfficial notice → - US
Randox Laboratories Ltd. recalls Randox Cholesterol- For the quantitative in vitro determination of Cholesterol in serum and plasma. Catalog Number: CH2O0
Product fails to meet the performance claims quoted on the kit insert: Manual Procedure when calibrating using the standard provided in the kit, the change in absorbance is lower than expected generating internal…
- US
Randox Laboratories Ltd. recalls Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD
A customer reported a problem with the reagent and calibrator. Randox Laboratories carried out an investigation and confirmed the issue. The complaint is pertaining to atypical calibration curves that can results in…
- US
CooperSurgical, Inc. recalls LifeGlobal Fast Freeze Thawing Kit, Model No. GFT5-055
There was translation error in the Spanish version of the IFU where the Spanish version instructs the user to leave the blastocyte to air thaw for 5 minutes rather than the correct 5 seconds as indicated in the English…
FDA · DeviceCooperSurgical, Inc.Domestic: USA AL, AZ, CA, CT, FL, GA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MT,…Official notice → - US
Ambu Inc. recalls Ambu VivaSight 2 DLT; endobronchial tube system used for verifying tube placement and repositioning. Catalog numbers 412351000, 412371000,…
Firm has received complaints on the device concerning leak/rupture of either the bronchial or tracheal cuff. Leakage during procedure could lead to loss of secure airway and will require re-intubation of patient.
FDA · DeviceAmbu Inc.Domestic distribution nationwide. Foreign distribution to Austria, Belgium,…Official notice → - US
DePuy Orthopaedics, Inc. recalls ATTUNE Measured Sizing and Rotation Guide-to size the femur and align rotation of the bone cuts in preparation for the femoral implant…
Manufactured with a Galvanized High Carbon Steel spring instead of the correct 302 Stainless steel spring. has the potential to oxidize and corrode in the ATTUNE Measured Sizing & Rotation Guide, resulting in surgical…
FDA · DeviceDePuy Orthopaedics, Inc.Nationwide Foreign: Argentina, Australia, Austria, Bahrain, Belgium, Brazil,…Official notice → - US
Smith & Nephew, Inc. recalls (1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186. (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left,…
The product was mispackaged (swapped). The devices within the inner tray matches the inner tray but does not match the outer box label and the chart sticks.
FDA · DeviceSmith & Nephew, Inc.US Nationwide distribution in the states of AZ, CA, GA, KS, LA, MN, MI, MO,…Official notice → - US
Baxter Healthcare Corporation recalls Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress, REF P7924A01; and REF P7924ARENT01, PRO+ MRS Rental Surface with X-Ray mattress.
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of…
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice → - US
Aesculap Implant Systems LLC recalls MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
- US
Aesculap Implant Systems LLC recalls Universal Robot UR5 arm, PV010204 subcomponent of Aesculap Aeos Digital Microscope System, PV010
Malfunction of the robotic arm preventing further movement of the robotic arm and requiring restart of the robotic digital microscope system.
- US
ROi CPS LLC recalls Nonsterile convenience kits: (1) regard Item #830099008, CV01005H - CV Part 1 Bundle; and (2) regard Item #830019017, CV00214Q - CV.
Some nonsterile components that were supposed to be sterile were packaged in nonsterile kits.
FDA · DeviceROi CPS LLCDistribution was made to MO. There was no foreign/military/government…Official notice → - US
Aesculap Implant Systems LLC recalls RIGHT CORONAL BENDER, TEK1940. Instrument used during spinal surgery.
Customized coronal rod benders may deform the implant when used with the spinal system devices.
- US
Xstrahl Limited recalls X80 RADiant Photoelectric Therapy System
There is a potential compatibility issue with the systems and replacement treatment applicators.
- US
RAYSEARCH LABORATORIES AB recalls RayStation 9B SP1. For radiation treatment planning.
An issue with propagation of treatment course information from RayStation with RayTreat to RayCare has been identified. During some workflows, information may not be propagated to RayCare.
FDA · DeviceRAYSEARCH LABORATORIES ABWorldwide distribution - US Nationwide distribution in the state of TN and the…Official notice → - US
Stryker Instruments Div. of Stryker Corporation recalls Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters)…
Some Canister Scanning Labels used to calibrate the Triton Canister System have a color variance. Based on a comprehensive analysis, blood loss estimates obtained using these Canister Scanning Labels may result in…
- US
Surgical Innovations Ltd recalls YelloPort Elite Universal Seal. For use in laparoscopic procedures.
There is the potential that YelloPort Elite Universal Seals packaging may contain small holes which may affect the sterility of the product.
FDA · DeviceSurgical Innovations LtdWorldwide distribution - US Nationwide distribution in the states of FL, IN,…Official notice → - US
Stryker Instruments Div. of Stryker Corporation recalls Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
Gauss Surgical is updating the Instructions for Use (IFU) for our Triton Sponge System in order to clarify proper technique for handling sponges and the calibration placard.
- US
Synapse Biomedical Inc recalls NeuRx Diaphragm Pacing System (NeuRx DPS), Affected part numbers: Part # Part Name 20-0035 NeuRx DPS System Kit 20-0036 NeuRx Diaphragm…
Firm has revised labeling to consistently call out storage conditions and revised the instructions for use to clarify that the temperature range symbol is intended to indicate storage conditions (versus transport…
FDA · DeviceSynapse Biomedical IncDomestic distribution to AL CA CO FL GA IL MA MI MN NC NJ NY OH OK OR PA SC TX…Official notice → - US
Boston Scientific Corporation recalls GreenLight HPSEA Laser Fibers, UPN 0010-2092
Several complaints were received for the affected lot; users received a "Fiber type does not match card type" error message on the GreenLight XPS Laser console, necessitating the replacement of the laser fiber and…
FDA · DeviceBoston Scientific CorporationDomestic distribution to AR CA IL ME MI NC TX Foreign distribution to…Official notice → - US
Aesculap Implant Systems LLC recalls ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during orthopedic…
Nonfunctional key due to the potential for damage to the key pins cause by force of use during assembly of the tibia locking ring.
FDA · DeviceAesculap Implant Systems LLCUS Nationwide distribution in the states of AL, AZ, CA, CO, ID, IL, LA, MA,…Official notice → - US
R & D Systems, Inc. recalls Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations…
The Instructions for Use (IFU, Part Number 750095) provided with the affected lots by the firm contains an error associated with product s CE marking. The CE mark contained in the IFU is followed by the Notified Body…
FDA · DeviceR & D Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of FL, MN,…Official notice → - US
GE Healthcare, LLC recalls GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia System, Part number…
There is a potential reversal of the O2 and air cylinder pressure transducer connections.
FDA · DeviceGE Healthcare, LLCWorldwide Distribution. US nationwide, Australia, Austria, Belgium, Bolivia,…Official notice → - US
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare, Catalog No. 7202
During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band. Kinking of the sheath may prevent the snare from fully closing, and injury may result.
FDA · DeviceHobbs Medical, Inc.Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.Official notice → - US
SONEX HEALTH LLC recalls SX-One MicroKnife
Potential of dull blade
FDA · DeviceSONEX HEALTH LLCUS Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, ID, IN,…Official notice → - US
Stryker Neurovascular recalls Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413;…
Microcatheter product label on the carton is missing the microcatheter product drawing/illustration.
FDA · DeviceStryker NeurovascularWorldwide distribution - US Nationwide distribution in the states of CA, OR,…Official notice → - US
- US
- US
Blount Fine Foods Corporation recalls Panera Bread at Home Southwest Corn Chowder, 16 oz. (453 g)
Contains undeclared wheat
FDA · FoodBlount Fine Foods CorporationMA, ME, IL, IA, OH, CA, MI, NH, WA, TX, VA, NYOfficial notice → - US
Tarts A La Carte, LLC dba Blazo Pie shoppe LLC recalls 9-inch pie Blazos Pie Shoppe Chocolate Peanut Butter Cream Pie (UPC 9438600049) 9-inch pie Blazos Pie Shoppe…
Blazos Pie Shoppe Peanut Butter Cream Pie, Chocolate Peanut Butter Cream Pie and Peanut Butter Cream Cup products possibly contaminated with Salmonella.
- US
Queen Bee Gardens, LLC recalls Honey Caramels Blue Raspberry. Product available in 5.87 oz. bag, 1 lb. bag, 3 lb. bag, 6 lb. bag. PLU Code for 5.87 oz. bag: 788394 12675…
Products may potentially contain one or more of the following undeclared tree nuts: Pecans, Almonds, Coconut, Macadamia Nuts, & Walnuts.
FDA · FoodQueen Bee Gardens, LLCTen retail locations owned by Queen Bee in CO, NM, WY and nationwide via…Official notice → - US
Chuckanut Bay Foods LLC recalls Item 35001-12, Chocolate Covered CHEESECAKE BITES NY SIGNATURE. Edible brand. Distributed by Wish Foods, LLC. Perishable - Keep…
Undeclared Soy Lecithin. Label declares Sunflower Lecithin instead of Soy Lecithin.
FDA · FoodChuckanut Bay Foods LLCDistributed in AL, CA, CO, FL, IL, MA, MI, MN, NY, OR, TX, WA, and WI.Official notice → - US
Chuckanut Bay Foods LLC recalls Item 34033-12, Chuckanut Bay Chocolate Covered Coconut Cheesecake Bites. Perishable - Keep Refrigerated. There are 8 pieces per pack and…
Undeclared Soy Lecithin. Label declares Chocolate Compound (Sunflower Lecithin) instead of Soy Lecithin.
FDA · FoodChuckanut Bay Foods LLCDistributed in AL, CA, CO, FL, IL, MA, MI, MN, NY, OR, TX, WA, and WI.Official notice → - US
Revive Organics, Inc. recalls Revie Superfoods Coconut Cream 190g Ready-to-Blend Coconut Delight Smoothie Made in Canada UPC 8 54681 00016 9 Revive Superfoods 1880…
Potential norovirus from IQF raspberries that were used as an ingredient in the products.
FDA · FoodRevive Organics, Inc.U.S. distribution to distributors located in PA, CA, IL, and TX who further…Official notice → - US
Loud Muscle Science recalls Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.
Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
FDA · DrugLoud Muscle ScienceThe product was distributed nationwide in the USA and Canada.Official notice → - US
Loud Muscle Science recalls Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.
Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
FDA · DrugLoud Muscle ScienceThe product was distributed nationwide in the USA and Canada.Official notice → - US
Amazon.com, Inc. recalls Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO ,…
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
- US
Apotex Corp. recalls Aripiprazole Tablets, USP 20 mg, packaged in a) 1,000-count bottle (NDC 60505-2676-8, UPC 3 60505 26768 2), b) 30-count bottle (NDC…
Failed dissolution specifications: OOS for dissolution at the 12-month stability time point.
- US
CIPLA recalls Difluprednate Ophthalmic Emulsion, 0.05%, 5ml bottles, Rx only, Mfd. by: Cipla Ltd., India At M/S Indoco Remedies Limited., L-32, 33, 34,…
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
- US
Glenmark Pharmaceuticals Inc., USA recalls Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark…
Failed Tablet/Capsule Specification : Capsule breakage
- US
- US
Vi-Jon, LLC recalls Hydrogen Peroxide Topical Solution USP, 3%, 16 FL OZ (1 PT) 473 mL bottle, packaged as a) Signature Care NDC 21130-871-43 UPC 3…
Cross Contamination With Other Products: Product is cross contaminated with low levels of isopropyl alcohol.
- 2022-07-26
- US
Spartan Fire, LLC: Electrical Load Center May Overheat
An overheated load center can increase the risk of a fire.
- US
E-One Incorporated: Electrical Load Center May Overheat
An overheated load center can increase the risk of a fire.
- US
Capacity of Texas: Steering Gear Assembled Incorrectly
A fractured steering gear can cause a loss of steering control, increasing the risk of a crash.
- US
Ferrari North America, Inc.: Loss of Brake Function
A loss of brake function can increase the risk of a crash.
Canada 29
- 2022-07-29
CA- CA
IMVAMUNE Vaccine: Updated Storage Conditions and Shelf Life
New safety information - Product safety
Health CanadaOfficial notice → - 2022-07-28
- CA
- CA
- CA
- CA
NUK First Choice Glass Baby Bottles Recalled due to Lead in Excess of Allowable Limit
Chemical hazard
Health CanadaOfficial notice → - CA
- CA
Powercom/Milcom Underwater Wireless Diver Units recalled due to Fire Hazard
Fire hazard
Health CanadaOfficial notice → - CA
- CA
Kidoozie Brand Play Tents recalled due to Potential Flammability Hazard
Flammability hazard
Health CanadaOfficial notice → - CA
Apotex recalls Apo-Acyclovir tablets due to a nitrosamine impurity
Contamination
Health CanadaOfficial notice → - 2022-07-27
- CA
- CA
- CA
Health Canada warns LIKCO Baby Walker may pose an injury hazard
Injury hazard
Health CanadaOfficial notice → - 2022-07-26
- CA
- 2022-07-25
- CA
Irresistibles brand Sesame Asian Style Dressing recalled due to spoilage
Non harmful (quality or spoilage)
- CA
- CA
Everflex Self-Expanding Peripheral Stent With Entrust Delivery System
Performance
Health CanadaOfficial notice → - CA
- CA
- CA
Hls Set Advanced 5.0 and 7.0 With Bioline Coating
Labelling and packaging
Health CanadaOfficial notice → - CA
- CA
Magnesium Citrate Oral Solution; Microbial contamination
Product quality
Health CanadaOfficial notice → - CA
- CA
- CA
- CA
- CA
- CA
United Kingdom 2
- 2022-07-29
- UK
Skechers Junior Effie Stripe Joggers Black sold via MandM Direct (2207-0174, 2207-0170, 2207-0172, and 2207-0173)
High risk of entrapment as the functional draw cord measures longer than the permissible limit of 20cm
- 2022-07-28
- UK
Elgetec & Something Cosmetics Ultrapower Ionic Hair Dryer sold via TK Maxx
Risk of electric shock and fire
Australia 2
- 2022-07-26
AUVarious Smoked Fish Products
Listeria monocytogenes may cause illness in pregnant women and their unborn babies, the elderly and people with low immune systems.
- 2022-07-25
- AU
Little Tikes 3-in-1 Activity Walker
If the locking pin disengages while the walker is in use it may collapse causing a child to fall, increasing the risk of an injury.
New Zealand 2
- 2022-07-28
NZMorgan Plus Four & Morgan Plus Six
Preliminary investigations indicate premature degradation of the rubber seal(s) in a third-party manufactured master cylinder. This may result in compromised brake performance, and in extreme cases cause brake failure.
Product Safety NZOfficial notice →- NZ
Boundaryline Fencing Systems - Tek Screws
There is a risk that the screws that hold the panel-bracket to the fence post may not be structurally sound and that the head of the screw(s) can break off allowing the panel brackets to come loose, and that ultimately…
Product Safety NZOfficial notice →
EU & EEA 27
- 2022-07-29
LTEUSoft toy
Small parts (metal pendant) can easily detach from the toy. As a consequence, a small child may put them in the mouth and choke. The product does not comply with the requirements of the Toy Safety Directive nor with…
EU Safety Gate · reported by LithuaniaOfficial notice →- LTEU
Body lotion (TREE HUT) · TREE HUT SHEA MOISTURIZING BODY LOTION Coconut Lime
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Body lotion (TREE HUT) · TREE HUT SHEA MOISTURIZING BODY LOTION Tropical Mango
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Shaving foam (FIGARO) · FIGARO Shaving Foam Regular Shave Classic
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Leave-on body spray (L.O.L. SURPRISE!) · L.O.L. Surprise! Colonia Corporal Body Spray
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
ROEUChildren's sweatpants (Setty Koop)
The trousers have long functional cords to be tied at the waist area. They can become trapped during various activities of a child, leading to injuries. The product does not comply with the requirements of the General…
- DEEU
Safety vest
The vest does not have a sufficient retroreflective surface. As a result, the user is not sufficiently visible in situations where high visibility is essential. The product does not comply with the Personal Protective…
EU Safety Gate · reported by GermanyOfficial notice → 
CZEUMagnetic balls · Magnetické kuličky Neocube 5 mm, 216 ks – zelená
The toy is made of small parts (balls) with a high magnetic flux. A child may put them in the mouth and ingest them, which may lead to choking if they enter the airways. If various are swallowed, they could attract one…
EU Safety Gate · reported by CzechiaOfficial notice →- LTEU
Moisturizing cream (seesee) · AURA ultra comfort MINERAL DAY MOISTURIZER DEAD SEA MINERALS FOR ALL SKIN TYPES
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Tanning cream (Soleo) · SUMMER NIGHT POWER BRONZER
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Face gel (belkosmex) · FACIAL GEL PLANT ADVANCED ALOE VERA HIALURON
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Body cream (Natura Siberica) · RICH SIBERIAN WHITE BODY BUTTER
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Face cream (FIGARO) · FACE CREAM AFTER SHAVE ANTI WRINKLE Q10
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Moisturizing cream (Peau D‘OR) · 365 HYDRATANT
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Tanning lotion (Peau D‘OR) · Ibiza black
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is forbidden in cosmetic products. BMHCA may harm the reproductive system, may harm the health of the unborn child…
- LTEU
Toy aeroplane · Flash/Electric plane fighter "Defender Aeronef"
Small parts (the wheels and stickers with plastic film) can easily detach from the toy. As a consequence, a small child may put them in the mouth and choke. The product does not comply with the requirements of the Toy…
EU Safety Gate · reported by LithuaniaOfficial notice → - FREU
Bus (BLUEBUS) · 12M IT3
Faulty positioning of the mylar insulating sheet (placed between 2 adjacent cells in the battery) may lead to a short circuit, increasing the risk of fire. The product does not comply with the requirements laid down in…
- DEEU
Body powder (Enchanteur) · Enticing Perfumed Talc
The product contains an excessive amount of arsenic (8.53 mg/kg). Arsenic is toxic and might cause cancer. The product contains an excessive amount of cadmium (0.56 mg/kg). Cadmium is harmful to human health because it…
NLEUToy set (Petilou / Le Toy Van) · Petilou Sensory Shapes
A small part of the activity shape with the green flower could become detached. The toy can easily break, resulting in small parts. A child may put them in the mouth and choke. The product does not comply with the…
- CYEU
Children's clothing set (EMERY KIDS)
The product contains long cords in the waist area that may become trapped during various activities of a child, leading to injuries. The product does not comply with the requirements of the General Product Safety…
- CYEU
Children's clothing set (EBITA)
The long decorative cords with free ends on the blouse can become trapped during various activities of a child, leading to injuries. The product does not comply with the requirements of the General Product Safety…
- DEEU
Passenger car (Mercedes-Benz) · GLE-Class
The screw connection of a 12V wiring harness pf the vehicles equipped with plug-in hybrid traction may have been secured with insufficient torque. As a result, the electrical resistance of the connection could increase…
- DEEU
Passenger car (Maserati) · Levante
Improperly attached ground cables of the 48 V motor can lead to electrical faults. As a result, sparks and the smell of burning may occur, which leads to an increased risk of fire. The product does not comply with the…
- DEEU
Safety vest (Sesam)
The vest does not have a sufficient retroreflective surface. As a result, the user is not sufficiently visible in situations where high visibility is essential. The product does not comply with the Personal Protective…
BGEUChildren's clothing set („BRAVA BABY“)
The small decorative stones glued on the blouse are easily detached and a child might put these in the mouth and choke on them. The product does not comply with the requirements of the General Product Safety Directive.
- DEEU
Particle filter mask (Famex) · FFP2 Famex - Modell Fago S 101 (nb 2841)
The particle/filter retention of the material is insufficient (measured values: as low as 81%). Consequently, the product does not fulfil the health and safety requirements; thus, even if combined with other…
- HUEU
USB charger (SENZHEN) · Bran Design
The insulation of the product is inadequate. The user could receive an electric shock from accessible (live) parts. The product does not comply with the requirements of the Low Voltage Directive nor with the standard…
Collected automatically from official sources. Check each official notice for exact models, batch codes and remedies. Disclaimer