Recalls in 2024
By month
Most recalled brands
By product type
- Drugs & medical1361
- Vehicles1098
- Food & drink525
- Toys & kids101
- Electrical51
- Other43
Recalls in the United States in 2024
- 2024-12-30
USWinnebago Industries, Inc.: Entrance Door Window May Detach
A window that detaches during transit can become a road hazard, increasing the risk of a crash.
- 2024-12-26
- US
GEM WAEV LLC: The Wheel May Separate From The Ball Joint
Ball joint separation can cause a loss of steering control, increasing the risk of a crash.
- US
BCI Burke Recalls Playground Merry-Go-Rounds Due to Crush Hazard
The space between the rotating platform and the stationary outer rim can leave a gap that narrows too much, posing a crushing hazard to children.
CPSCPlaydale Playgrounds LTD, of United KingdomAbout 415 (In addition, about 6 were sold in Canada)Official notice → - US
GIKPAL Dressers Recalled Due to Tip-Over and Entrapment Hazards; Violations of Federal Regulation for Clothing Storage Units; Sold Exclusively on Walmart.com by ONME…
The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate performance and warning…
- US
Precor Recalls Resolute™ Cable Multi-Station Exercise Equipment Due to Impact Injury Hazard
The pop-pin can fail to fully engage in the exercise equipment's vertical rail and cause the pulley carriage to drop unexpectedly during use, posing an impact injury hazard to users.
- US
Black Diamond Equipment Recalls PIEPS Pro IPS Avalanche Transceivers Due to Risk of Loss of Emergency Communications
The battery compartment within the avalanche transceiver could not have enough contact force to supply power. In some cases, the transceiver will fail to power on or cease operating during use. It would make it…
- 2024-12-25
- US
Mint Medical GmbH recalls mint Lesion, Software Versions: 3.9.0 through 3.9.5.
Some software versions have a malfunction where they may show incorrect orientation labels for a specific subset of DICOM images.
FDA · DeviceMint Medical GmbHWorldwide distribution: US (nationwide): AR, CA, FL, GA, MI, MN, NY, OH, PA,…Official notice → - US
Olympus Corporation of the Americas recalls Duravent Silicone Ventilation Tube. Model Number: 240075.
Potential that Duravent Silicone Ventilation Tubes may contain incorrect product, specifically, 1.32 mm Tiny T Tubes (model: 70240076) instead of the intended Duravent Silicone Ventilation Tubes.
FDA · DeviceOlympus Corporation of the AmericasAL, AZ, CA, IL, KY, MD, MN, MO, NC, ND, NY, OK, PA, SC, TN, TX, WA, WI.…Official notice → - US
GE OEC Medical Systems, Inc recalls OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging system used to…
Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability.
FDA · DeviceGE OEC Medical Systems, IncU.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA,…Official notice → - US
Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HOT DOG PATIENT WARMING, Temperature Management Controller, Multiport, Models: 1) Model # WC77, 2)…
Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
- US
MicroPort Orthopedics Inc. recalls EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE…
Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect packaging.
- US
MEDLINE INDUSTRIES, LP - Northfield recalls HUDSON RCI mBrace, ET Tube Holder with 4 Point Head Strap, REF DYNJMBRC4; tracheal tube fixation device
Complaint defects have been noted regarding the adhesive elements of the device and the frame of the holder putting additional pressure on the patient's cheekbones and upper lip which may cause dermal injury depending…
- US
Noah Medical recalls Galaxy System (GAL-001)
Bronchoscopic system uninterruptable power may have defective component, may cause power supply short circuit/trip protective circuit breakers causing sudden, unrecoverable power loss, which could occur while system is…
FDA · DeviceNoah MedicalUS: CA, MA, PA, NJ, ID, CT, MO, NC, MD, IL, TN, VA, OH, IN, WV, NYOfficial notice → - US
CooperSurgical, Inc. recalls Brand Name: K-Systems Product Name: G85 Mini Incubator Model/Catalog Number: K22074 Software Version: N/A Product Description: An…
The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will alarm appropriately.
FDA · DeviceCooperSurgical, Inc.States: NC, NJ, TX, VA, IL, NY, CA, PA Please note: The countries below,…Official notice → - US
Philips North America Llc recalls Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216
The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the client device to…
- US
Spacelabs Healthcare, Ltd. recalls Eclipse PRO REF 98700 The Spacelabs model 98700 is a portable non-invasive Holter recorder intended to record the patient s ambulatory…
Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder. The physical serial number label on the device might not match the serial number programmed into the…
FDA · DeviceSpacelabs Healthcare, Ltd.U.S.: AR, CA, CO, DE, FL, FA, LA, MA, MI, MN, MT, NC, NE, NU OH, OR, PA,…Official notice → - US
Spectranetics Corporation recalls Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm OTW 417-152 /…
Due to complaints received for the marker band detaching from the distal tip of the catheter and remaining in the patient as laser catheter was retracted.
FDA · DeviceSpectranetics CorporationU.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, ILIN, KS, KY,…Official notice → - US
Draeger Medical, Inc. recalls Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in…
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
FDA · DeviceDraeger Medical, Inc.No Atlan A300 or A300XL devices were imported into the US. Devices were direct…Official notice → - US
Medtronic Neurosurgery recalls Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM VCATH 35CM 27636 EDM 27636 EXACTA W/BRAIDED CORD LOCK 27666…
Due to complaints received reporting cracks and/or leaks of the stopcocks associated with the external drainage and monitoring system (EDMS).
FDA · DeviceMedtronic NeurosurgeryWorldwide distribution. US nationwide including Puerto Rico; Algeria,…Official notice → - US
Kirwan Surgical Products, LLC recalls Optikon Bipolar Pencil 25 Gauge Straight. Model/Catalog Number: OPT14-5011. Product Description: The Disposable Microsurgical…
Potential for the outer stainless-steel tube to break or detach.
FDA · DeviceKirwan Surgical Products, LLCWorldwide - US Nationwide including PUERTO RICO; AUSTRALIA, CANADA, CHILE,…Official notice → - US
- US
Rise Baking Company, LLC dba The New French Bakery Inc. recalls L'Oven Fresh KETO Friendly Original 6 Tortilla Wraps. Net Wt. 7.8 oz(222g) UPC 4099100271348. Dist &…
Foreign Material (metal)
FDA · FoodRise Baking Company, LLC dba The New French Bakery Inc.CT, KS, MN, OH, TXOfficial notice → - US
GRIFFITH FOODS LTD recalls Item 42081001, 104023600 SPICY BREADING EXPORT, 50 lb. bag
potential for pieces of metal in product
- US
Field Fresh Foods, Inc. recalls Fresh Creative Foods, raw cucumber diced (1/4 cubes.) with skin, Net Wt. 20lbs. (4x5lbs.)
Cucumbers possibly contaminated with Salmonella; associated with outbreak
- US
Terry and Joe Baker Farms, LLC dba Baker Farms recalls Baker Farms CURLY MUSTARD 16 oz NET WT 16 oz UPC 8 13098 02018 4 Baker Farms 3667 Ellenton-Norman Park Road…
The firm was notified by the Texas Department of Agriculture that the product test positive for Listeria monocytogenes.
FDA · FoodTerry and Joe Baker Farms, LLC dba Baker FarmsProduct was shipped to distribution centers in the following states: AL, AR,…Official notice → - US
Stuyvers Bread (Premium Brand Bakery Division) recalls Baguette, Artisan Multigrain. (30 Units/box) 400g/each. Contains: Wheat, Sesame Seeds, Gluten (rye, barley, oat)…
Possible contamination by a foreign object (metal) in sub-ingredient in dinner roll product
FDA · FoodStuyvers Bread (Premium Brand Bakery Division)product was distributed to two consignees in 3 different states (California,…Official notice → - US
SE Tampa Inc dba Tampa Food recalls Crab Cheese Rangoon, NET WT: 8 LB, 120 pieces of 30g / 3 Trays per master cardboard boxes, Keep Frozen, packaged in corrugated…
Undeclared allergens: Milk, Soy, Crustacea Shellfish, Fish
- US
Ocean Group Inc. recalls SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB SALMON NORWAY 6/7KG FR NOR F LB SALMON BAKKAFROST FAROE ISLANDS 6/7KG FR FRO F LB SALMON…
Potential for contamination of Listeria monocytogenes. Environmental sample collected by FDA yielded positive results for one Zone 1 (cutting board) and one Zone 3 (floor drain).
FDA · FoodOcean Group Inc.Various retail and restaurant establishments in California.Official notice → - US
- US
F&S Fresh Foods, Inc. recalls WHOLE FOODS MARKET, Organic Carrots & Celery, NET WT. 15 oz (425 g), PERISHABLE KEEP REFRIGERATED, Packed For: Whole Foods Market Austin,…
Potential contamination with E. coli O121:H19
- US
Fabalish, recalls Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard tray inside plastic film inside cardboard box, individual units
Potential E Coli contamination.
FDA · FoodFabalish,CA, CO, FL, GA, IL, IN, KS, MA, MT, NE, NH, NY, OH, TN,TX, UT, VA, WAOfficial notice → - US
Compass Minerals America Inc. recalls Bulk salt product shipped in 1 metric ton tote; 50lb bag Special Purity Granulated Food-Grade Salt with UPC 041582150158; 44lb bag…
foreign material
FDA · FoodCompass Minerals America Inc.Product distributed to Canadian customers and US customers in MA, IN, WIOfficial notice → - US
Impossible Foods Inc recalls Impossible Spicy Ground Sausage Meat from plants 14oz chub, UPC 8 16697 02109 5; 8 retail chubs per case
product may contain pieces of metal
- US
Macleods Pharmaceuticals Ltd recalls Olanzapine Tablets, USP 2.5 mg, 30-count bottle, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540,…
Failed Impurities/Degradation Specifications
- US
- US
Apothecus Pharmaceutical Corp. recalls VCF, Vaginal Contraceptive Gel, Birth Control, 10 Pre-filled Applicators, Net Wt. 0.09 oz (2.55g) Each, Distributed By: Apothecus…
CGMP deviations: out of specifications for assay
FDA · DrugApothecus Pharmaceutical Corp.Nationwide in the USA and 2 Distributors in Hong KongOfficial notice → - US
- US
Aurobindo Pharma USA Inc recalls Nebivolol Tablets, 2.5. mg, 30-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East…
CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-Nitroso Nebivolol above acceptable intake (AI) limit.
- US
Keystone Industries recalls Gelato, Benzocaine 20% Topical Gel Anesthetic Gel, Net Wt. 1 oz. (30ml), Manufactured by Keystone Industries 480 S. Democrat Rd.,…
CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was…
FDA · DrugKeystone IndustriesNationwide in the USA and Canada, Dominican Republic, El Salvador, Honduras,…Official notice → - 2024-12-24
- US
Tesla, Inc.: Air Bag May Tear During Deployment/FMVSS 208
A torn air bag may not adequately protect an occupant in a crash, increasing the risk of injury.