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 2 minutes ago
United States
Audio Partnership Recalls Cambridge Audio Yoyo (M) Portable Bluetooth Speakers Due to Fire Hazard
The lithium-ion batteries in the Cambridge Audio Yoyo (M) Portable Bluetooth Speaker can overheat, posing a fire hazard.
Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Loyoda Direct and Loyoda
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and…2024 Toyota Tacoma Hybrid and other models recall: Incorrect load carrying capacity on Label/FMVSS 110
A vehicle with an incorrect maximum capacity weight value may be overloaded, increasing the risk of a crash.2026 C-HR battery electric vehicles recall: Loss of drive power from software programming error
An unexpected loss of drive power increases the risk of a crash.Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT with software V4.5&V5.0
Potential of failing to trigger clinical scan during Bolus Tracking.FUJIFILM Healthcare Americas Corporation recalls FUJIFILM Synapse PACS software v7.4.310
Software issue may cause the ruler measurement to be inaccurate.Healthmark Industries Co., Inc. recalls healthmark ProChek-II and 1 more products
Test manufactured with an expired ingredient which may present as either a false negative or positive.ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B…
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.Henry Schein Inc. recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm and 1 more products
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S.Midmark Corporation recalls Midmark IQecg Digital ECG and 1 more products
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.Hollister Ulc recalls Onli 17cm Hydrophilic Urethral Intermittent Catheter
Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to…Medline Industries, LP recalls Medline medical convenience kit labeled as: TRACH TUBE KIT
Component labeling discrepancyGE Medical Systems Information Technologies Inc recalls PORTRAIT CORE SERVICES SOFTWARE V1.1 and 3 more products
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer.American Contract Systems Inc recalls American Contract System Convenience Kit and 3 more products
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays.AVID Medical, Inc. recalls Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR… and 1 more products
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.Medline Industries, LP recalls Medline medical convenience kits and 3 more products
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential…Canon Medical System, USA, INC. recalls Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital…
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.Merge Healthcare, Inc. recalls Merge PACS and Merge OrthoPACS
Software issue may cause measurements to be displayed inaccurately.Fresenius Medical Care Renal Therapies Group, LLC recalls Fresenius Medical Care
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar…Olympus Corporation of the Americas recalls POWERSEAL 5 MM
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.Medline Industries, LP recalls Medline Hudson RCI and 2 more products
Neonatal and infant heated wire breathing circuits may experience sporadic failure.IMRIS Imaging Inc recalls ORT200 and 1 more products
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked…Medline Industries, LP recalls Medline convenience kits labeled as: 1) FEMORAL PACK and 10 more products
Kits contain a potentially contaminated component which were recalled by the manufacturerA little guidance
Get more from your tools
Practical guide 3 min read
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.
Practical guide 3 min read
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.