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 26 minutes ago
United States
Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by Gudook Outdoor Sports
The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation and certification…2024 Valkyrie vehicles built with track suspension recall: Brake master cylinder seal may deform
Brakes that overheat increase the risk of a fire.2026 Entegra Qwest and other models recall: False taillight warning light on instrument panel Display/FMVSS 101
The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.2026 Entegra Qwest SE and other models recall: False taillight warning light on instrument panel Display/FMVSS 101
The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.Abiomed, Inc. recalls Automated Impella Controller
A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns.Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker
Incorrect inner package labeling.O&M Halyard Inc recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771
Nitrile Exam Glove failed to meet specifications chemical permeation performance.Philips Medical Systems Nederland B.V. recalls Azurion system and 1 more products
It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service.Medtronic Neuromodulation recalls Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation and 1 more products
A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.Bolton Medical Inc. recalls RelayPro Thoracic Stent-Graft System
Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.Medline Industries, LP recalls Medline medical convenience kit labeled as EYE TRAY-LF
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile.Abiomed, Inc. recalls Automated Impella Controller
Retrospective submission for following issues identified: 1.Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection and 6 more products
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including…GE Medical Systems Information Technologies Inc recalls GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL and 5 more products
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and…AbbVie Inc. recalls PRED MILD
Failed Stability SpecificationsAVEVA Drug Delivery Systems, Inc. recalls Nicotine Transdermal System Patch
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of…Fly By Jing Inc. recalls Fly By Jing
Possible cross-contamination resulting in undeclared allergen ingredient (Peanut)Honeyville, Inc recalls
Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.Wawa Beverage Company recalls Wawa Iced Tea Lemon 16 oz Pint and 3 more products
Undeclared Milk Allergen,Legacy Bakehouse LLC recalls Butter Parsley Bagel Crisps and 2 more products
Products were made with recalled California Dairies milk powder due to Salmonella.1997-2002 and other models recall: Low brake air pressure warning light may not Illuminate/FMVSS 121
A low brake air pressure warning light that fails to illuminate when the engine is off will not alert the driver to a low brake pressure condition, increasing the risk…2027 Telluride and other models recall: Driver seat belt strap may not Extend/FMVSS 209
A seat belt strap that does not extend can fail to restrain an occupant in a crash, increasing the risk of injury.2026 Ram ProMaster vehicles equipped with Q'Straint's One-Combo Belt and other models recall: Wheelchair seat belts may not properly restrain occupants
Improperly restrained occupants have an increased risk of injury during a crash.A little guidance
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What to do if something you own is recalled
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