Recalls in 2022
By month
Most recalled brands
By product type
- Drugs & medical1804
- Vehicles1690
- Toys & kids1129
- Food & drink946
- Electrical589
- Other503
All recalls in 2022
- 2022-12-30
UK- UK
- UK
Portable Fan Heater sold via Amazon, eBay, Fruugo, Gumtree and U-Buy
Serious risk of electric shock
- UK
- UK
- UK
- UK
- UK
- UK
- UK
Iceland Foods recalls Mars Dessert Bar because of undeclared peanut and egg
Of undeclared peanut and egg
CA- CA
- CA
- CA
- CA
- CA
- CA
- CA
- 2022-12-29
USIndian Motorcycle Company: Kickstand May Not Retract Properly/FMVSS 123
A kickstand that does not properly retract can increase the risk of a crash.
- US
Volkswagen Group of America, Inc.: 12-Volt Battery Cable May Short Circuit
A short circuit may cause a loss of drive power, increasing the risk of a crash. A short circuit also increases the risk of a vehicle fire.
- US
Hendrickson USA. L.L.C.: Loose Brake Pad Retaining Clip May Damage Tire
A retaining clip or bracket that detaches can damage the brake pad, reducing brake performance, damage a tire valve, causing a flat tire, or become a road hazard, increasing the risk of a crash.
- US
JD E-Commerce America Limited: Child Seat May Be Improperly Installed/FMVSS 213
The child seat may be improperly installed, increasing the risk of injury in a crash.
- US
Yamaha Recalls Viking Off-Road Side-by-Side Vehicles Due to Crash and Injury Hazards (Recall Alert)
Improper installation of the retaining bolts could result in the parking brake mechanism failing to hold the vehicle when parked allowing the vehicle to move unintentionally, posing crash and injury hazards.
- US
ZLINE Recalls Gas Ranges Due to Serious Risk of Injury or Death from Carbon Monoxide Poisoning
The oven of the gas ranges can emit dangerous levels of carbon monoxide (CO) while in use, posing a serious risk of injury or death from carbon monoxide poisoning.
- US
Surf 9 Recalls Body Glove Tandem and ULI Inflatable Paddle Boards Due to Drowning Hazard; Sold Exclusively at Costco
The glue on the inflatable paddle boards can separate at the seams and the paddle boards can deflate unexpectedly, posing a drowning hazard.
CPSCJiangxi Aike Outdoor Sports, of ChinaAbout 13,300 (In addition, about 7,000 of the Body Glove…Official notice → - CA
Various Spirit Police Uniform Costume Hats recalled due chemical hazard
Chemical hazard
Health CanadaOfficial notice → - 2022-12-28
- US
Tomy International Inc. recalls Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L
Affected lots of the product are being recalled due to potential microbial growth in the fluid inside the device. if a compromised product is used by a child with a weakened immune system, an infection or other illness…
FDA · DeviceTomy International Inc.Worldwide distribution - US Nationwide and the countries of Canada, Australia,…Official notice → - US
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box,…
Scissors contained debris.
FDA · DeviceMedical Action Industries, Inc. 306Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no…Official notice → - US
Baxter Healthcare Corporation recalls Revaclear 300 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
Reports of Polyurethane Displacement in the dialyzer, and might be identified as a blood leak
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the countries of Canada, China,…Official notice → - US
Baxter Healthcare Corporation recalls Revaclear 400 Dialyzer. Product Code: 114749M. Not distributed in the USA. Used to treat chronic and acute renal failure by…
Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer
FDA · DeviceBaxter Healthcare CorporationWorldwide distribution. US Nationwide including Guam and St. Thomas USVI;…Official notice → - US
GE Medical Systems, LLC recalls Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes,…
Potential for batteries that have not been replaced at 2 years, as recommended in the Service Manual, they can fail or possibly emit smoke, or catch fire.
FDA · DeviceGE Medical Systems, LLCWorldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice → - US
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
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FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the state of VA.Official notice → - US
Heartware, Inc. recalls HeartWare Model 1100
Over time, the driveline cover may become hardened, creating difficulty or an inability to slide the cover back to access the driveline to controller connector. Access to the driveline connector may be delayed, which…
- US
Companion Medical, Inc. recalls InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA, MMT-105ELPKNA, MMT-105NNBLNA,…
Diabetes management app may crash immediately upon opening, while using the app and/or while app is running in the background, which may lead to inability to use the app. An error message may be displayed indicating…
FDA · DeviceCompanion Medical, Inc.US Nationwide distribution including in the states of CA, NY, MT, OH, IN, MN,…Official notice → - US
Abbott Molecular, Inc. recalls Abbott Alinity m Resp-4-Plex Amp Kit, Part Number 09N79-096
Reports of an increase in reactive negative controls and false positive results with certain lots of Alinity M Resp-4-Plex AMP kits.
- US
NuVasive Inc recalls X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Potential that insert will be unable to disengage from the vertebral body replacement device/implant
FDA · DeviceNuVasive IncWorldwide - U.S. Nationwide distribution including in the states of NC, CA,…Official notice → - US
Howmedica Osteonics Corp. recalls Full Dose CE Simplex P Single Bone Cement - Indicated for the fixation of prostheses to living bone in orthopaedic Catalog Number:…
Instructions for Use (IFU) included in the packaging is missing a translation in the Turkish language. Although the Turkish translation is missing, all content within the IFUs is accurate.
FDA · DeviceHowmedica Osteonics Corp.International distribution in the country of Turkey.Official notice → - US
Natus Medical Incorporated recalls The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set that is used to…
Due to Cranial Access Kits containing recalled sterile surgical drapes. The sterile surgical drapes are being recalled due to the liner on the adhesive component is difficult to remove without damaging the product and…
FDA · DeviceNatus Medical IncorporatedU.S. Nationwide distribution in the states of AK, CA, CT, DC, FL, GA, IA, ID,…Official notice → - US
Fresenius Medical Care Holdings, Inc. recalls 2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute and chronic dialysis therapy in a healthcare…
(1)Software version 2.74 upgrade and (2)hardware related cause that affects only CDX Machines, has been identified as the UI-MICs Board is sensitive to Electromagnetic Interference (EMI) which will cause the false…
- US
GE Medical Systems, LLC recalls B105P Patient Monitor (with E-module slot option), REF 6160000-001-XXXXXX,
GE Healthcare has become aware that if certain B1x5P / B1x5M patient monitors use "mmHg" or "kPa" as the unit for CO2 measurement, the displayed value for CO2 measurement can be inaccurate when used in a location that…