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.
3,836 recalls, newest first · Checked 16 minutes ago
United States
GBYMIUY Recalls Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
The magnetic stick figure toy sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children.
Designs Direct Recalls Cupcakes and Cashmere Brand Three-Light Floor Lamps, Due to Risk of Serious Injury from Fire and Burn Hazards
When plugged in or switched on, the lamp cord or internal wiring can smoke, melt, spark, overheat or ignite, posing a risk of serious injury from fire and burn hazards.
Agrish Reannounces and Expands Recall of Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Additional Units Added
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within…
Gazelle USA Recalls Urban Arrow Cargo Electric Bikes Due to Fall Hazard
The front bolt in the seat post clamping mechanism can break, causing the seat to become loose, posing a fall hazard.2026-2027 Anthem AN (4) and other models recall: Intake and grille bezels may detach
A detached bezel can become a road hazard for other vehicles, increasing the risk of a crash.Saint Francis Apizza LLC Issues a Voluntary Recall of its Frozen Pizzas for Missing Sub Ingredients on the Label for Soy Which Includes Soybean Oil and Soy Lecithin, an Allergen
Undeclared soy allergen
Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk
Potential to be contaminated with Listeria monocytogenes2018-2024 EV Star and other models recall: Bus may move with wheelchair lift deployed
The bus moving while the wheelchair lift is in use increases the risk of injury.2023-2026 ID.4 recall: High voltage battery may catch fire
A vehicle fire increases the risk of injury.Baxter Healthcare Corporation recalls Brand Name: VOLARA System Product Name: VOLARA
Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate.Becton, Dickinson and Company recalls ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The…
Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.Seaspine Orthopedics Corporation recalls SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head
The proximal thread depth of the spinal device is out of design specification.Philips Ultrasound, LLC recalls Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Due to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood flow…Maquet SAS recalls PowerLED 300 Concealed Lighting System
The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.CooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name:
A small number of lenses within the affected lot are of the incorrect power.Boston Scientific Corporation recalls Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5
Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature.Cardinal Health 200, LLC recalls Presource Convenience Kits: 1) KIT and 1 more products
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator.AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE and 1 more products
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.Baxter Healthcare Corporation recalls PRO+ MRS SURFACE FOR VERSACARE and 2 more products
There is an error in the product description on the Unique Device Identification (UDI) label.DeRoyal Industries Inc recalls REF: 81-030415 Myocardial Probe Non-Pyrogenic
Myocardial temperature probes contain an incorrect needle.AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.New York Embroidery Studio, Inc. recalls New York Embroidery Studio Trinity Non-Surgical Isolation Gown
Gowns do not consistently meet the minimum liquid-barrier performance required.Ventec Life Systems, Inc. recalls HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve and 2 more products
Labeling; Oxygen Cylinders do not contain required medical gas labelingA 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.
Practical guide 3 min read
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.