Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,853 recalls, newest first · Checked 5 minutes ago
United States
BRP Recalls Can-Am All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury and Death from Crash Hazard
The ATV's speed limiter control can malfunction, causing unexpected speed and acceleration, posing a serious risk of injury or death from crash hazard.
Amazon Recalls Amazon Basics 55 Lbs. Adjustable Dumbbells Due to Impact Hazard
The weight plates can fail to engage completely during weight adjustment and dislodge from the dumbbell handle when used, posing an impact hazard.Waltco MDV series liftgates recall: Liftgate deck pins may break
A liftgate that falls unexpectedly increases the risk of injury.Weldon UV800 Display Unit user interfaces and other models recall: Touch screen display may fail
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash.2024-2025 Air vehicles equipped with rear-wheel drive recall: Inverter may fail and cause a loss of drive power
A loss of drive power increases the risk of a crash.BioFire Diagnostics, LLC recalls Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
Respiratory/sore throat panel test may result in false negative results and control failures.Mint Medical GmbH recalls Mint Lesion
If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or…Intuitive Surgical, Inc. recalls Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
Reloads for curved-tipped stapler may potentially produce an incomplete staple line.Cook Incorporated recalls Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use… and 2 more products
Marker bands may be at an increased risk of cracking/breakage.Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe…Intuitive Surgical, Inc. recalls Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X
Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.Orthorebirth Co Ltd recalls BioCera Fibers and 1 more products
Resorbable bone void filler falls outside standard specifications.Erbe Medical, LLC recalls ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources and 2 more products
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to…Boston Scientific Corporation recalls LUX-DX II and 1 more products
For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring…BioFire Diagnostics, LLC recalls BioFire Joint Infection
Contamination to in-vitro diagnostic test may result in false positives.Ventec Life Systems, Inc. recalls VOCSN V+Pro package
Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during…Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps and 11 more products
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.Spacelabs Healthcare, Inc. recalls Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module…
Due to a manufacturing issue (i.e.American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating…
Impacted kits contain syringes recalled by Medline Industries.Physio-Control, Inc. recalls LIFEPAK 15
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was…Centinel Spine, Inc. recalls Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement. and 1 more products
Product labeling mix up.DFI Co., Ltd. recalls One Step 10A in vitro diagnostic test and 6 more products
The devices were distributed without required FDA premarket clearance or approval.AVID Medical, Inc. recalls Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05 and 9 more products
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and…A little guidance
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Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
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How to check if your car has a recall
Find the recalls for your make and model, confirm with your VIN whether your car is affected, and know what do-not-drive and park-outside warnings mean.
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What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.