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 7 minutes ago
United States
Dissolved Oxygen Test Kits Recalled Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Almpal
The recalled test kits contain a bottle of sulfuric acid, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act.
Blossom Recalls Children's Loungewear Due to Serious Risk of Injury or Death from Burns; Violates Mandatory Standard for Children's Sleepwear
The recalled children's loungewear sets violate the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries or death to children.2021-2022 LEAF vehicles equipped with a Level 3 quick charging port recall: Fire risk from quick charging battery
A quick charging battery that overheats increases the risk of a fire.2025 Tacoma and other models recall: Driveshaft may deform and break
A broken driveshaft can impair steering.2022-2025 Tundra and other models recall: Rearview camera image may not Display/FMVSS 111
A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.2026 Model Y recall: Reverse lights may fail to Illuminate/FMVSS 108
Reverse lights that fail to illuminate reduce visibility and may not alert pedestrians or other drivers that the vehicle is backing up, increasing the risk of a crash.Ethicon, LLC recalls STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device
Potential for barb non-engagement.Boston Scientific Corporation recalls Extractor Pro RX Retrieval Balloon Catheter
The product in incorrectly labeled.Mindray DS USA, Inc. dba Mindray North America recalls BeneVision N1 Patient Monitor
Potential for activation of an abnormal alarm pause.Biofire Defense recalls FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative
FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead to delayed results…Biomet, Inc. recalls Juggerknot Mini Soft Anchors
The outer carton box label is for the JuggerKnot 1.0mm Mini products.CooperVision, Inc. recalls MyDay Toric and 2 more products
One lot manufactured with an invalid sterilization cycle.Ortoma Ab recalls Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001…
Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel and 9 more products
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.Stryker Communications recalls Chromophare Surgical Light System
Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.Abiomed, Inc. recalls Automated Impella Controller
Specific Automated Impella Controllers (AICs) that have a Pump Driver Circuit Assembly do not meet current specifications.Maquet Cardiovascular, LLC recalls Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW…
Reports of out-of-box failures discovered during the limited launch phase.MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY and 1 more products
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to…Philips Medical Systems Nederland B.V. recalls Allura Xper FD10 Product Codes: and 12 more products
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit).Tandem Diabetes Care, Inc. recalls t:slim X2 Insulin Pump with Interoperable Technology
an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to…Baxter Healthcare Corporation recalls Baster Continu-Flo Solution Set
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing…Yangzhou Yulou Paper Products Co., LTD recalls Quick Touch Alcohol Prep Pads
cGMP DeviationsMedline Industries, LP recalls READYPREP PVP
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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.