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 10 minutes ago
United States
Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures
The recalled gates violate the mandatory standard for expansion gates and expandable enclosures because a child's torso can fit through the opening between the gate and…2025 Altima and other models recall: Improperly welded door Strikers/FMVSS 206
A door that opens unexpectedly while the vehicle is in motion increases the risk of injury or a crash.2026 Explorer recall: Inadequate windshield Bonding/FMVSS 212
In the event of a crash, windshield detachment can increase the risk of injury.2025 F-59 and other models recall: Brake lights may fail to Illuminate/FMVSS 108
Brake lights that do not illuminate properly while driving increase the risk of a crash.2025-2026 Fuzion and other models recall: Ramp door may break during use
A ramp door that breaks during use increases the risk of injury.2025 NGDV recall: Wheel may detach from vehicle
A detached wheel can cause a loss of vehicle control or become a road hazard for other vehicles, increasing the risk of a crash.2023-2024 ID.4 recall: Park outside - high voltage battery may catch fire
A vehicle fire while parked or driving can increase the risk of injury.a 2022 and other models recall: Loss of vehicle control from loose axle clamp fasteners
A loss of vehicle control increases the risk of a crash.2023-2025 ID.4 recall: High-Voltage battery may overheat and cause fire
A high-voltage battery that overheats increases the risk of a fire.C-Rad Positioning Ab recalls Brand Name: Catalyst+ Product Name: Catalyst
Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups.Boston Scientific Corporation recalls Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter
Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter…Medtronic Inc recalls Abre Venous Self-Expanding Stent System
Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force.ICU Medical, Inc. recalls Plum Duo Infusion System
ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound.Thoratec LLC recalls CentriMag Blood Pump
Acute circulatory support system pump may not fit into the motor and reports received of the pump not being securely locked into the motor using the screw-in locking…Instrumentation Laboratory recalls The product is used for the evaluation of the intrinsic coagulation pathway
Potential for microbial contamination.Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Emphasizing instructions for LVP duration programming located in the IFU.Philips Medical Systems Nederland B.V. recalls Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the…
Six (6) identified software issues which may result in the following: system keeps restarting, AMC triple drive, C-Partition of Suite PC running out of free space…Ge Medical Systems Israel, Functional Imaging recalls SMV DSX New Line and 3 more products
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in…Hologic, Inc recalls ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.
Fungal contamination of affected lot with Parengyodontium album.Abbott Diabetes Care, Inc. recalls FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3… and 3 more products
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose resultsDiagnostica Stago, Inc. recalls Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for…
Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results.ICU Medical Inc. recalls Pulsator Arterial Blood Sampling Kit and 1 more products
Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery.Repligen Corporation recalls MAVERICK¿ Measurement Module Spectrometer PN 820-01367
Potential Elevated Laser Output A disconnected cable or a poorly crimped cable under mechanical bending stress can cause loss of electrical contact.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.
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.