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 7 minutes ago
United StatesMedical Action Industries, Inc. 306 recalls Kit: Epidural/Pain TQC 20/Cs and 1 more products
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.Windstone Medical Packaging, Inc. recalls AMS Convenience Kit: DSAEK Pack
The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have…HeartSine Technologies Ltd recalls HeartSine SAM 350P 350P US Device
Due to a damaged (over stretched) membrane tail that causes an intermittent fault.Atrium Medical Corporation recalls Getinge PVC Thoracic Catheter and 2 more products
An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.C.R. Bard Inc recalls Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF… and 5 more products
Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.Lutronic Corporation recalls Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that…
Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.Nipro Renal Soultions USA, Corporation recalls MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 and 3 more products
Hemodialysis concentrates contain high endotoxin levelsB Braun Medical Inc recalls 0.9% Sodium Chloride Injection
Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyreneBaxter Healthcare Corporation recalls Dextrose Injection
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.Ajanta Pharma USA Inc recalls Fluphenazine Hydrochloride Tablets
Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability.American Regent, Inc. recalls Epinephrine Injection
Presence of Particulate Matter and Lack of Assurance of Sterility.ImprimisRx NJ LLC recalls Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution
Subpotent DrugOurPharma LLC recalls fentaNYL Citrate
Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry…
A&P Creations LLC Issues Nationwide Recall of X10 Natural Enhancement Supplement Due to Undeclared Sildenafil and Tadalafil
Product contains sildenafil and tadalafilCentric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels
Elevated Endotoxin levelB Braun Medical Inc recalls Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number…
Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump and 1 more products
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI)…Fresenius Medical Care Renal Therapies Group, LLC recalls GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B and 2 more products
Complaints of blue-green discoloration in productMedos International Sarl recalls Velys Enabling Tech Robotic-Assist Station REF: 451611001
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear and 12 more products
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete…Philips North America Llc recalls Philips Brilliance. Models: Brilliance iCT and 3 more products
Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the…Boston Scientific Corporation recalls LUX-Dx and 2 more products
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs).Johnson & Johnson Surgical Vision, Inc. recalls HEALON EndoCoat PRO
Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered during…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.