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 5 minutes ago
United StatesBeckman Coulter Inc. recalls DxC 500 AU Module w/ISE
On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the…bioMerieux, Inc. recalls VITEK¿ 2 Gram-negative AST Test Kits
Potential for false resistant results for Colistin (cs02n) with multi-drug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii complex used in specific cardsLeMaitre Vascular, Inc. recalls Artegraft Collagen Vascular Grafts Model Numbers:
The bovine carotid arteries used to produce the impacted grafts from affected lots were sourced using raw material from a supplier that had not been reviewed and…Medline Industries, LP recalls Medline Kits: 1) VALVE PACK-LF
The kits contain certain lots of cannula products where the catheter may not retain its shape.Change Healthcare Canada Company recalls Change Healthcare Radiology Solutions software version 14.2.2
Due to software issue, radiology reports may not be fully displayed when viewing.Howmedica Osteonics Corp. recalls 1. EXETER V40 STEM 44MM NO 2
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa.Medline Industries, LP recalls Sterile Medline Convenience Kits: 1) MAJOR PACK L-F and 1 more products
Convenience kits labeled as sterile have not gone through the sterilization process.Schiller, Ag recalls Argus PB-3000
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the…Getinge Disinfection Ab recalls Getinge 88-Series Washer- Disinfector. Model Number: 88-5.
Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure…Aesculap AG recalls AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R. and 1 more products
Mislabeling.Philips Medical Systems Nederland B.V. recalls Allura Xper FD10C and 14 more products
The BIOS battery may deplete faster than initially anticipated during the design phase.Medline Industries, LP recalls Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH… and 4 more products
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates.Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software… and 1 more products
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.Zap Surgical Systems recalls ZAP-X Radiosurgery System
If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error message occurs after…MedicalCommunications GmbH recalls Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0
Potential that the measured value may be smaller than the actual area.Northeast Scientific Inc. recalls NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number… and 7 more products
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.North American Rescue LLC. recalls JUNCTIONAL EMERGENCY TREATMENT TOOL
Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of…Siemens Medical Solutions USA, Inc recalls Biograph mMR. Model Number: 10433372. and 14 more products
There is a potential for an ice blockage to form or currently exist within the magnet venting system.Medtronic MiniMed, Inc. recalls Medtronic
The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection.Amerisource Health Services LLC recalls Carbamazepine Extended-Release Tablets
Failed Dissolution Specifications.Apotex Corp. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution and 1 more products
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concernsZydus Pharmaceuticals (USA) Inc recalls Entecavir Tablets and 1 more products
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurityOven Artisans llc recalls Orwashers brand Soho Sourdough XL Batard
Mislabeled: Product may contain undeclared sesame seedsA 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.