Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 4 minutes ago
ReCor Medical Inc. recalls Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿…
Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.Abiomed, Inc. recalls Purge Cassette
Increased risk of purge leaks with Generation 1 purge cassettes.Medline Industries, LP recalls ENFIT G-TUBE CONNECTOR and 1 more products
Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Enzymatic Hemoglobin A1c
A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer.Olympus Corporation of the Americas recalls Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE… and 1 more products
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to…Abiomed, Inc. recalls Automated Impella Controller
Potential that the "Purge System Blocked" alarm display on the Automated Impella Controller (AIC) could be delayed when using first generation Impella 5.5 (0550-0008*)…Oxoid Australia Pty Limited recalls OXOID MICROBACT IDENTIFICATION KITS
Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result…BD Kiestra Lab Automation recalls BD Kiestra" ReadA
In certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface.Synthes (USA) Products LLC recalls 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. and 1 more products
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect…Intuitive Surgical, Inc. recalls Brand Name: da Vinci S and 3 more products
Due to increased complaints for broken/frayed grip cables for reusable instruments.Philips Medical Systems Nederland B.V. recalls Allura Xper FD10C and 21 more products
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.Mentor Texas, LP. recalls CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: 354-9113 and 6 more products
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.Burlington Medical, LLC recalls Burlington Medical and 12 more products
Potential for attenuation degradation over time, decreasing the lifespan.Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 12G and 7 more products
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers.Medtronic MiniMed, Inc. recalls MiniMed 670G Insulin Pump and 13 more products
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when…Intuitive Surgical, Inc. recalls Brand Name: da Vinci S and 1 more products
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instrumentsGE Healthcare LLC recalls SIGNA Premier systems
Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel)…Medline Industries, LP recalls Airway Exam Kit and 6 more products
Kits contain recalled Olympus biopsy valves.Alembic Pharmaceuticals, Inc. recalls Bromfenac Ophthalmic Solution 0.07%
Failed Impurities/Degradation Specifications: out of specification at the time of testing i.e.K.C. Pharmaceuticals, Inc recalls Sterile EYE DROPS AC and 7 more products
Lack of Assurance of SterilityAmneal Pharmaceuticals, LLC recalls Magnesium Sulfate in Water for Injection
Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.Amneal Pharmaceuticals, LLC recalls traMADol Hydrochloride Tablets
Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval during…Appco Pharma LLC recalls Prazosin Hydrochloride Capsules and 2 more products
cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.A 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.