Recall roundup: 5 Sep – 11 Sep 2022

94 official recalls and safety alerts were published in the week of 5 Sep – 11 Sep 2022, down 24% on the week before (124). Most were drugs & medical (28) and food & drink (17); common issues included choking hazard (10), food allergen (7), baby product (3). 10 were flagged as serious.

Recalls this week

94

5 Sep – 11 Sep 2022

By country

  1. United States47
  2. Canada16
  3. United Kingdom7
  4. Australia2
  5. EU & EEA22
  6. Austria5
  7. Germany5
  8. Hungary4
  9. Poland2
  10. Ireland2

By product type

  1. Drugs & medical28
  2. Food & drink17
  3. Toys & kids17
  4. Vehicles15
  5. Other4
  6. Home & garden4

Most recalled brands

  1. Aroma King2
  2. BMW2
  3. Clinical Innovations2

Common searches

  1. Choking hazard10
  2. Food allergen7
  3. Baby product3
  4. Listeria3
  5. E-cigarette2
  6. Battery1

Most serious

Recalls the agency classed as serious, or with a risk of death, fire, electric shock, drowning or strangulation.

  1. 2022-09-09
  2. CA
  3. 2022-09-08
  4. US
    Home & garden

    Murphy Beds Recalled Due to Serious Impact and Crush Hazards; Manufactured by Cyme Tech (Recall Alert)

    The wall beds can break or detach from the wall and fall onto those nearby, posing serious impact and crush hazards.

    CPSCCyme Tech, of CanadaAbout 8,200Official notice →
  5. AU
    Home & garden

    KM8020 III Karma Eagle Wheelchair

    Users may be misinformed about the safe user weight of the chair, increasing the risk that the user may be seriously injured if the wheelchair breaks or collapses, or if the user falls out of the chair.

  6. 2022-09-07
  7. US
    Drugs & medicalClass I

    Medtronic Xomed, Inc. recalls NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306

    The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.

    FDA · DeviceMedtronic Xomed, Inc.Worldwide distribution: US (nationwide) and OUS (foreign) countries of:…Official notice →
  8. US
    Food & drinkClass I

    Lyons Magnus, Inc recalls kate farms Peptide 1.5 Cal/mL, Plain, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 51823-00646 1. 12 count case UPC…

    Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

    FDA · FoodLyons Magnus, IncNationwideOfficial notice →
  9. US
    Food & drinkClass I

    Supherb Farms recalls IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock, CA Perishable, Keep Frozen

    RTE Frozen Dill is being recalled after a customer tested product and Listeria Monocytogenes was found to be present

    FDA · FoodSupherb FarmsNationwide and CanadaOfficial notice →
  10. US
    Food & drinkClass I

    Epicurean Butter Co. recalls Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with a sealed lidding film under the lid. Best By and Lot #…

    Firm's supplier of frozen dill notified firm of a recall due to potential contamination with Listeria monocytogenes.

    FDA · FoodEpicurean Butter Co.Wegmans Food Markets in MA, MD, NC, NJ, NY, PA, VA, DC.Official notice →
  11. US
    Food & drinkClass I

    Raw Seafoods Inc. recalls Lemon Dill Butter Pucks

    Firm used dill recalled for Listeria monocytogenes to product butter pucks

    FDA · FoodRaw Seafoods Inc.OH, MAOfficial notice →
  12. 2022-09-06
  13. UK
    Toys & kidsSafety report

    4moms MamaRoo Swing and RockaRoo Rocker

    Strangulation hazard as the restraint straps can dangle below the seat and non-occupant crawling infants can become entangled in the straps. 4moms have launched a strap fastener replacement programme

  14. UK
    Toys & kidsRecall

    Queen West Trading Co. Baby Blanket in Blue and Beige

    Risk of entrapment, strangulation, and choking due to the loose threads around the edge of the blanket

United States 47

  1. 2022-09-08
  2. US
    VehiclesVehicle

    Ford Motor Company: Wheel Lug Nuts Not Tightened Correctly

    Incorrectly tightened wheel lug nuts can loosen and result in wheel separation from the vehicle, increasing the risk of a crash.

    NHTSAFord Motor Company1,519 affectedOfficial notice →
  3. US
    VehiclesVehicle

    Terex South Dakota, Inc.: Platform Leveling Cylinder Support Welds Failure

    A platform that tips during use increases the risk of an injury.

    NHTSATerex South Dakota, Inc.194 affectedOfficial notice →
  4. US
    VehiclesVehicle

    Volkswagen Group of America, Inc.: Fuel Tank Vent Pipe May Be Damaged

    A damaged vent pipe may allow fuel to spill out of the filler neck when the fuel cap is opened, increasing the risk of an injury.

    NHTSAVolkswagen Group of America, Inc.13,004 affectedOfficial notice →
  5. US
    VehiclesVehicle

    BMW of North America, LLC: Horn Not Attached Securely

    A loose or partially detached horn can interfere with motorcycle steering and increase the risk of a crash.

    NHTSABMW of North America, LLC252 affectedOfficial notice →
  6. US
    Home & garden

    Murphy Beds Recalled Due to Serious Impact and Crush Hazards; Manufactured by Cyme Tech (Recall Alert)

    The wall beds can break or detach from the wall and fall onto those nearby, posing serious impact and crush hazards.

    CPSCCyme Tech, of CanadaAbout 8,200Official notice →
  7. US
    Sports & outdoor

    Tethrd Recalls One Stick GEN 2 Climbing Sticks Due to Fall and Injury Hazards (Recall Alert)

    Under pressure, one or more of the climbing stick's steps can crack causing them to break, posing fall and injury hazards to users.

    CPSCAbout 7,700Official notice →
  8. US
    Home & garden

    Roots & Harvest Wide Mouth Pint Canning Jars Recalled by LEM Products Distribution Due to Laceration Hazard

    Pieces of glass can be found in some of the recalled jars, posing a laceration hazard to consumers.

    CPSCAbout 15,900Official notice →
  9. US
    Toys & kids

    Hearing Lab Technology/Lucid Audio Recalls Children's HearMuffs Due to Burn and Injury Hazards from Rupturing Alkaline Batteries

    The AAA alkaline batteries included in the recalled HearMuffs can rupture, posing hearing, projectile and/or burn injury.

    CPSCAbout 31,150Official notice →
  10. 2022-09-07
  11. US
    VehiclesVehicle

    Nissan North America, Inc.: Unsecured Transmission May Cause Rollaway

    A vehicle rollaway increases the risk of a crash.

    NHTSANissan North America, Inc.197,230 affectedOfficial notice →
  12. US
    VehiclesVehicle

    BMW of North America, LLC: Third-Row Seat Springs Improperly Installed

    In a crash, the seat backrest may not fully lock, increasing the risk of injury.

    NHTSABMW of North America, LLC246 affectedOfficial notice →
  13. US
    Drugs & medicalClass II

    Oculus Optikgeraete GMBH recalls Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.

    Due to a software issue, IOL calculator printout often does not accurately reflect the alignment axis and incision position when planning toric IOLs

    FDA · DeviceOculus Optikgeraete GMBHU.S.: AL, AR, AZ, CAQ, CO, CT, FL, GA, HI, IA, ID, IL, KS, KY, MD, ME, MI, MN,…Official notice →
  14. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls The PRM is intended to be used as part of the ZOOM LATITUDE Programming System to communicate with Boston Scientific implantable…

    There is potential for unanticipated software anomalies to occur when using the Model 2868 Application loaded on the 3120 ZOOM LATITUTDE programmer when communicating with certain Boston Scientific transvenous…

    FDA · DeviceBoston Scientific CorporationWorldwide DistributionOfficial notice →
  15. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors

    Procedure packs contained a recalled product.

    FDA · DeviceDeRoyal Industries IncUS Nationwide distribution in the states of OH and TN.Official notice →
  16. US
    Drugs & medicalClass II

    Corin Ltd recalls TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.

    Some of the devices did not pass fatigue testing.

    FDA · DeviceCorin LtdDistribution was made to NJ. There was no military/government distribution.Official notice →
  17. US
    Drugs & medicalClass II

    Canon Medical System, USA, INC. recalls INFX-8000V. For radiographic and fluoroscopic studies and intervention.

    The fluoroscopic dose rate might exceed the conforming value during biplane fluoroscopy.

    FDA · DeviceCanon Medical System, USA, INC.US Nationwide DistributionOfficial notice →
  18. US
    Drugs & medicalClass II

    Abbott Laboratories recalls ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27

    One lot of reagent was manufactured with insufficient quantities of the heterophilic blocking agents in the conjugate component.

    FDA · DeviceAbbott LaboratoriesNationwideOfficial notice →
  19. US
    Drugs & medicalClass II

    Qiagen Sciences LLC recalls FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010

    Increased occurrence rate of false positive results, lead to a false positive sample result that could subsequently be incorrectly reported from the laboratory. A false positive result could lead to the risk of the…

    FDA · DeviceQiagen Sciences LLCIN, NC, MN, TX Foreign: Belgium, China, Germany, Jordan, Italy, Netherlands,…Official notice →
  20. US
    Drugs & medicalClass II

    New Standard Device Inc recalls Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill Half-Pin…

    Complaints were received for Self-drill Half-Pin tip breakages occurring during surgery.

    FDA · DeviceNew Standard Device IncU.S.: AZ, GA, IL MT, NC, NJ, NV, OH, PA, TX, and VA O.U.S.: NoneOfficial notice →
  21. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3.…

    Negative bias with patient samples. The mean patient sample bias range from -26% to -33%,potential risk of delay in appropriate treatment and management decisions.

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide distribution - US Nationwide and the countries of Canada, Austria,…Official notice →
  22. US
    Drugs & medicalClass II

    Siemens Medical Solutions USA, Inc recalls Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700

    Siemens has become aware of a potential hardware issue with Artis Q, Artis Q.zen, Artis pheno and Artis icono systems with a specific lot of X-ray tubes. In rare cases, if the error detection mechanism fails, it will…

    FDA · DeviceSiemens Medical Solutions USA, IncWorldwide Distribution: US (nationwide) and OUS (Foreign) to countries of:…Official notice →
  23. US
    Drugs & medicalClass II

    Medtronic Inc. recalls EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System

    Update to IFU provides a manual deployment workaround method to help mitigate potential harms related to partial stent deployment.

    FDA · DeviceMedtronic Inc.worldwideOfficial notice →
  24. US
    Drugs & medicalClass II

    OXFORD IMMUNOTEC LTD recalls T-Cell Xtend REF TTK.610 US

    Due to equipment failure, affected products were stored at temperatures outside the validated range of 2-8 degree C for a period longer than the validated storage time.

    FDA · DeviceOXFORD IMMUNOTEC LTDU.S.: AL, CA, DC, GA, IN, OR, and WA O.U.S.: NoneOfficial notice →
  25. US
    Drugs & medicalClass II

    bioMerieux, Inc. recalls VITEK 2 / MYLA VITEK 2 Software versions 8.01, 8.02 (veterinary use only), 9.01, 9.02, 9.03 MYLA Software versions V4.8 and V4.9

    There are 7 reported software anomalies that may affect use of the device.

    FDA · DevicebioMerieux, Inc.International distribution to the countries of Estonia, Bahrain, Pakistan, UK,…Official notice →
  26. US
    Drugs & medicalClass II

    Aggredyne, Inc. recalls AggreGuide A-100 Instrument

    The firm identified a software design issue where the improper shut down of the instrument resulted in speeds.csv file contents of the software version 5.1 being erased. Due to this issue, the target RPM for the assay…

    FDA · DeviceAggredyne, Inc.International distribution to the country of South Korea.Official notice →
  27. US
    Drugs & medicalClass II

    Aesculap Implant Systems LLC recalls Aesculap ENNOVATE SET SCREW STERILE-implants are used for dorsal monosegmental and multisegmental stabilization of the lumbar,…

    Potential for the incorrect screw to be included in the package.

    FDA · DeviceAesculap Implant Systems LLCGA, TXOfficial notice →
  28. US
    Drugs & medicalClass II

    Philips North America Llc recalls DigitalDiagnost C50 1.1

    Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, operators will see an incorrect orientation of the image on the first examination due to an issue in…

    FDA · DevicePhilips North America LlcNationwide Distribution including Puerto RicoOfficial notice →
  29. US
    Drugs & medicalClass I

    Medtronic Xomed, Inc. recalls NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229308 b) REF 8229307 c) REF 8229306

    The firm received reports of events related to airway obstruction while using NIM Standard Reinforced EMG Endotracheal Tubes & NIM CONTACT Reinforced EMG Endotracheal Tubes.

    FDA · DeviceMedtronic Xomed, Inc.Worldwide distribution: US (nationwide) and OUS (foreign) countries of:…Official notice →
  30. US
  31. US
    Food & drinkClass II

    Clinical Innovations, LLC recalls Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered…

    Firm received complaints of leaking, black liquid, and black particulates in the product vials.

    FDA · FoodClinical Innovations, LLCNationwide - all 48 states plus Washington DC and Puerto Rico. Australia and…Official notice →
  32. US
    Food & drinkClass II

    South Georgia Pecan Company recalls Great Value Chopped Walnuts, NET WT 4oz (113g); Ingredients: Walnuts DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716;…

    The firm stated that pecan pieces were packaged in pouches labeled as walnuts.

    FDA · FoodSouth Georgia Pecan CompanyProduct was shipped to distribution centers in North Carolina and Florida.Official notice →
  33. US
    Food & drinkClass II

    Clinical Innovations, LLC recalls Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptically packaged…

    Firm received complaints of leaking cups, black liquid, and black particulates in the 24% Sucrose Solution.

    FDA · FoodClinical Innovations, LLCNationwide.Official notice →
  34. US
    Food & drinkClass III

    Yem Foods LLC recalls Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen

    undeclared wheat starch sub-ingredient found in the asafoetida used in the products

    FDA · FoodYem Foods LLCCT, DE, IL, IN, KY, MA, MI, NC, NH, NJ, NY, OH, PA, TN, WIOfficial notice →
  35. US
  36. US
    Food & drinkClass I

    Lyons Magnus, Inc recalls kate farms Peptide 1.5 Cal/mL, Plain, Sole-Source Nutrition Formula. 325 mL (11 fl oz) UPC 8 51823-00646 1. 12 count case UPC…

    Findings and potential for Cronobacter sakazakii and Clostridium botulinum.

    FDA · FoodLyons Magnus, IncNationwideOfficial notice →
  37. US
    Food & drinkClass I

    Supherb Farms recalls IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock, CA Perishable, Keep Frozen

    RTE Frozen Dill is being recalled after a customer tested product and Listeria Monocytogenes was found to be present

    FDA · FoodSupherb FarmsNationwide and CanadaOfficial notice →
  38. US
    Food & drinkClass I

    Epicurean Butter Co. recalls Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with a sealed lidding film under the lid. Best By and Lot #…

    Firm's supplier of frozen dill notified firm of a recall due to potential contamination with Listeria monocytogenes.

    FDA · FoodEpicurean Butter Co.Wegmans Food Markets in MA, MD, NC, NJ, NY, PA, VA, DC.Official notice →
  39. US
    Food & drinkClass I

    Raw Seafoods Inc. recalls Lemon Dill Butter Pucks

    Firm used dill recalled for Listeria monocytogenes to product butter pucks

    FDA · FoodRaw Seafoods Inc.OH, MAOfficial notice →
  40. US
    Food & drinkClass II

    Woodland Foods LLC recalls Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice, 25 lbs. bag UPC…

    possible presence of glass pieces

    FDA · FoodWoodland Foods LLCAZ CA CT FL GA IL IN MA ME MI MN MO MT NC NH NJ NY OH SD TX VA WA WIOfficial notice →
  41. US
    Drugs & medicalClass II

    Padagis US LLC recalls Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed By Perrigo, Allegan, MI…

    CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.

    FDA · DrugPadagis US LLCNationwide in the USAOfficial notice →
  42. US
    Drugs & medicalClass II

    Tsm Brands LLC recalls Luxury 70% Isopropyl Alcohol, 16 FL. OZ. (1 PT) 473 ML, Distributed by: TSM Brands LLC, 540 Equinox Ln, Manalapan, NJ 07726, UPC…

    Labeling: Product Contains Undeclared API - product contains undeclared ethyl alcohol

    FDA · DrugTsm Brands LLCDistributed in VA, USAOfficial notice →
  43. US
    Drugs & medicalClass II

    Teva Pharmaceuticals USA Inc recalls Neomycin Sulfate Tablets, USP 500 mg , 100-count bottles, Rx only, Distributed by: TEVA PHARMACEUTICALS USA, INC North Wales, PA…

    CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.

    FDA · DrugTeva Pharmaceuticals USA IncNationwide within the United StatesOfficial notice →
  44. US
    Drugs & medicalClass III

    LNK International, Inc. recalls Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count blisters per carton, Distributed by: CVS Pharmacy, Inc., One CVS…

    Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.

    FDA · DrugLNK International, Inc.Product was distributed to one retailer who may have further distributed the…Official notice →
  45. US
    Drugs & medicalClass III

    Akorn, Inc recalls Timolol Maleate Ophthalmic Solution, USP, 0.5%, 5 x 0.3 mL Single-Dose Vials, Rx Only, Sterile, Manufactured for: Akorn, Inc., Lake…

    Failed Impurities/Degradation Specifications: Identification of an unknown impurity at the 12-month stability point.

    FDA · DrugAkorn, IncDistributed Nationwide in the USAOfficial notice →
  46. US
    Drugs & medicalClass II

    Family Dollar Stores, Llc. recalls Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0…

    cGMP deviation: Product held outside of appropriate temperature storage conditions.

    FDA · DrugFamily Dollar Stores, Llc.Distributed Nationwide in the USA to the following States: AZ, CA, GA, ID, IN,…Official notice →
  47. 2022-09-06
  48. US
    VehiclesVehicle

    Alamo Group Inc.: Hose Reel Assembly Failure

    A falling hose reel can increase the risk of an injury.

    NHTSAAlamo Group Inc.150 affectedOfficial notice →
  49. US
    VehiclesVehicle

    Keystone RV Company: Electric Stabilizer Jack Switch May Short

    An electrical short can cause the stabilizer jacks to extend during transit, increasing the risk of crash or injury.

    NHTSAKeystone RV Company536 affectedOfficial notice →
  50. US
    VehiclesVehicle

    Forest River, Inc.: Secondary Emergency Exit Missing

    A missing secondary exit could result in occupants becoming trapped inside during an emergency, increasing their risk of injury.

    NHTSAForest River, Inc.49 affectedOfficial notice →

Canada 16

  1. 2022-09-09
  2. CA
    Vehicles

    Harley-Davidson motorcycle recall: powertrain (Transport Canada 2016333)

    Problem area: powertrain. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.

    Transport CanadaOfficial notice →
  3. CA
    Vehicles

    Harley-Davidson motorcycle recall: brakes (Transport Canada 2016420)

    Problem area: brakes. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.

    Transport CanadaOfficial notice →
  4. CA
    Vehicles

    Harley-Davidson motorcycle recall: powertrain (Transport Canada 2017284)

    Problem area: powertrain. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.

    Transport CanadaOfficial notice →
  5. CA
    Vehicles

    Harley-Davidson motorcycle recall: brakes (Transport Canada 2018058)

    Problem area: brakes. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.

    Transport CanadaOfficial notice →
  6. CA
  7. CA
  8. CA
  9. CA
  10. 2022-09-08
  11. CA
  12. CA
    Drugs & medicalType II

    K360 Scalpel Handle

    Performance

    Health CanadaOfficial notice →
  13. CA
    Drugs & medicalType II

    Power Knee

    Performance

    Health CanadaOfficial notice →
  14. 2022-09-07
  15. CA
    Vehicles

    Subaru SUV recall: other (Transport Canada 2022435)

    Problem area: other. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.

    Transport CanadaOfficial notice →
  16. CA
  17. 2022-09-06
  18. CA
    Vehicles

    Honda motorcycle recall: fuel supply (Transport Canada 2017527)

    Problem area: fuel supply. The Transport Canada notice lists the affected models and model years, and what the manufacturer will do.

    Transport CanadaOfficial notice →
  19. CA
  20. CA

United Kingdom 7

  1. 2022-09-09
  2. UK
  3. 2022-09-08
  4. UK
  5. 2022-09-07
  6. UK
    Home & gardenRecall

    Smilatte Travel Mug

    Burns hazard as the mug base may fall away from the cup and cover user in very hot liquid.

  7. 2022-09-06
  8. UK
    Toys & kidsSafety report

    4moms MamaRoo Swing and RockaRoo Rocker

    Strangulation hazard as the restraint straps can dangle below the seat and non-occupant crawling infants can become entangled in the straps. 4moms have launched a strap fastener replacement programme

  9. UK
    Toys & kidsRecall

    Queen West Trading Co. Baby Blanket in Blue and Beige

    Risk of entrapment, strangulation, and choking due to the loose threads around the edge of the blanket

  10. UK
    ElectricalSafety report

    Nikon Monarch HG 10x42; & Monarch M5 10x42 Binoculars

    Chemical risk as the straps associated with a range of Nikon products have been reported as being in breach of the REACH Regulations by having excess PAH's

  11. UK

Australia 2

  1. 2022-09-08
  2. AU
    Home & garden

    KM8020 III Karma Eagle Wheelchair

    Users may be misinformed about the safe user weight of the chair, increasing the risk that the user may be seriously injured if the wheelchair breaks or collapses, or if the user falls out of the chair.

  3. AU
    Tools & DIY

    DeWalt DHS780 and DWS780-XE 305mm Mitre Saws

    If the plastic rear guard hits the rotating saw blade, fragments of the guard may hit the user or bystanders, causing injury.

EU & EEA 22

  1. 2022-09-09
  2. SKEU
    Clothing & jewellerychemical

    Ring

    The product contains lead (measured value 21,11 % by weight). Lead is harmful to human health, accumulates in the body and may affect breast-fed or unborn children. The product also releases an excessive amount of…

    EU Safety Gate · reported by SlovakiaOfficial notice →
  3. ATEU
    Toys & kidschoking

    Soft toy

    Small parts can easily detach (the eyes). 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 the European standard EN 71-1.

    EU Safety Gate · reported by AustriaOfficial notice →
  4. PLEU
    Electricalenvironment

    Power supply (LAMEX) · Zasilacz antenowy elektroniczny z gniazdem F

    The solder contains an excessive amount of lead (measured value upto 41,5% by weight). Lead poses a risk to the environment. The product does not comply with the requirements of the Directive on the restriction of the…

    EU Safety Gate · reported by PolandLAMEXOfficial notice →
  5. CZEU
    Toys & kidschemical

    Plastic doll (Pretty girl) · BEAUTIFUL Beautiful stories start from here

    The plastic material of the head of the doll contains an excessive concentration of di-(2-ethylhexyl) phthalate (DEHP) (measured value up to 4.84 % by weight).This phthalate may harm the health of children, possibly…

    EU Safety Gate · reported by CzechiaPretty girlOfficial notice →
  6. HUEU
    Toys & kidschemical

    Plastic doll set (Torch.hu (on the label)) · Játék baba / Panenka

    The product contains an excessive concentration of di-2-ethylhexyl phthalate (DEHP) (measured value: 25% by weight). This phthalate may harm the health of children, possibly causing damage to their reproductive system.…

    EU Safety Gate · reported by HungaryTorch.hu (on the label)Official notice →
  7. HUEU
    Toys & kidschemical

    Plastic doll with accessories (HUA YA (on label: Torch.hu)) · Kitchen Good helper

    The doll's head contains an excessive concentration of di- (2-ethylhexyl) phthalate (DEHP) and dibutyl phthalate (DBP) (measured values up to 28% and 0,54% by weight, respectively). These phthalates may harm the health…

    EU Safety Gate · reported by HungaryHUA YA (on label: Torch.hu)Official notice →
  8. HUEU
    Toys & kidschemical

    Plastic doll (Cute Girl) · Cute Girl

    The product contains an excessive concentration of di-2-ethylhexyl phthalate (DEHP) (measured value 33% by weight). This phthalate may harm the health of children, possibly causing damage to their reproductive system.…

    EU Safety Gate · reported by HungaryCute GirlOfficial notice →
  9. IEEU
    Otherchemical

    Disposable electronic cigarette (Aroma King) · Aroma King AK5500

    The product contains an excessive volume of nicotine-containing liquid. This could lead to the accidental consumption of a high dose of nicotine. Nicotine is acutely toxic in high doses and its inhalation can cause…

    EU Safety Gate · reported by IrelandAroma KingOfficial notice →
  10. IEEU
    Otherchemical

    Disposable electronic cigarette (Aroma King)

    The product contains more than the maximum permitted concentration of nicotine (announced value: 50 mg/ml) and is presented in a container that is too big.Nicotine is acutely toxic and can endanger the user’s safety,…

    EU Safety Gate · reported by IrelandAroma KingOfficial notice →
  11. HUEU
    Toys & kidschemical

    Plastic doll with accesiores (Manny, Torch) · Fashion Beautiful Girl

    The product contains an excessive concentration of di-2-ethylhexyl phthalate (DEHP) (measured value: 35% by weight). This phthalate may harm the health of children, possibly causing damage to their reproductive system.…

    EU Safety Gate · reported by HungaryManny, TorchOfficial notice →
  12. FREU
    Tools & DIYinjuries

    Agricultural tractor (CLAAS) · Arion 400

    The parking brake may not engage or may disengage, due to a technical fault. This can lead to that the tractor cannot be immobilised, increasing the risk for an accident. The product does not comply with the Regulation…

    EU Safety Gate · reported by FranceCLAASOfficial notice →
  13. DEEU
    Otherchoking

    Soother holder (Firtink)

    The product can easily break, releasing small parts. A small child may put them in the mouth and choke. The product does not comply with the requirements of the General Product Safety Directive nor with European…

    EU Safety Gate · reported by GermanyFirtinkOfficial notice →
  14. DEEU
    Otherchoking

    Soother holder (Bubuyun)

    The wooden beads break easily and generate small parts. A small child could put them in the mouth and choke. The product does not comply with the requirements of the General Product Safety Directive nor with the…

    EU Safety Gate · reported by GermanyBubuyunOfficial notice →
  15. DEEU
    Sports & outdoorchemical

    Fitness gloves (Chiba Gloves for Sports)

    The product contains chromium (VI) (measured value up to 17.5 mg/kg). Chromium (VI) is sensitising in contact with the skin, can trigger allergic reactions and may cause cancer. The product does not comply with the…

    EU Safety Gate · reported by GermanyChiba Gloves for SportsOfficial notice →
  16. NOEU
    Food & drinkenvironment

    Food thermometer · Food thermometer / Digitalt steketermometer

    The metal (solder) in the thermometer contains an excessive concentration of lead (measured value up to 55,2 %). Lead poses a risk to the environment. The product does not comply with the requirements of the Directive…

    EU Safety Gate · reported by NorwayOfficial notice →
  17. ATEU
    Toys & kidschoking

    Puffer toy · Megafüßler

    Small parts (eyes) can easily detach. A small child may put them in the mouth and choke on them. The product does not comply with the requirements of the Toy Safety Directive nor with the European standard EN 71-1.

    EU Safety Gate · reported by AustriaOfficial notice →
  18. DEEU
    Toys & kidsinjuries

    Baby carrier (Belly Boon)

    The carrier does not secure a baby sufficiently from falling to the ground. The carrier bends sideways or forwards and a baby may slip out and suffer fatal injuries. The product does not comply with the requirements of…

    EU Safety Gate · reported by GermanyBelly BoonOfficial notice →
  19. ATEU
    Toys & kidschoking

    Pull-along toy · Pull-along Giraffe

    Small parts (horns) can easily detach. 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 European standard EN 71-1.

    EU Safety Gate · reported by AustriaOfficial notice →
  20. ATEU
    Toys & kidschoking

    Soft toy · PES D&P

    Small parts (beads) can easily detach. 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 the European standard EN 71-1.

    EU Safety Gate · reported by AustriaOfficial notice →
  21. ATEU
    Toys & kidschoking

    Wooden rattle · Windel vip

    The product can easily break, releasing small parts. 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 the European standard EN 71.

    EU Safety Gate · reported by AustriaOfficial notice →
  22. DEEU
    Clothing & jewellerychemical

    Piercing jewellery (J-Club International) · Piercingschmuck

    The product releases an excessive amount of nickel (measured value up to 4.9 μg/cm²/week). Nickel is a strong sensitizer and can cause various allergic reactions if it occurs in objects that come into direct and…

    EU Safety Gate · reported by GermanyJ-Club InternationalOfficial notice →
  23. PLEU
    Toys & kidsdamage to sight, injuries

    Toy gun (PRO KIDS) · AIR GUN

    The kinetic energy of the arrows ejected is too high, exceeding the permitted levels. This can cause injuries to the child, in particular to the eyes. The product does not comply with the requirements of the Toy Safety…

    EU Safety Gate · reported by PolandPRO KIDSOfficial notice →

Collected automatically from official sources. Check each official notice for exact models, batch codes and remedies. Disclaimer