Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 2 minutes ago
United StatesStryker Medical Division of Stryker Corporation recalls Stryker MV3 bariatric bed and 1 more products
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a…GE Medical Systems, LLC recalls Senographe Pristina
Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR ¿1020.30(j).Bard Peripheral Vascular Inc recalls Safe-T-Centesis 6 Fr Catheter Drainage Tray
Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show…Philips North America recalls Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL…
Between July 2024 and June 2025, Philips Azurion R3.0 systems with a FlexArm stand were shipped without the Source-to-Skin Distance (SSD) Spacer.Draeger, Inc. recalls ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conduction of… and 3 more products
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.Cardinal Health 200, LLC recalls ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve
Affected gowns have the incorrect expiration date on the product packaging.Beckman Coulter, Inc. recalls Access 2 Reaction Vessels
It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities.Orthofix U.S. LLC recalls Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer… and 5 more products
Labeling contains claims that are not consistently present.C.R. Bard Inc recalls Bard InLay Optima Size: 6 Fr. x 14 cm and 3 more products
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.Steris Corporation recalls AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The… and 1 more products
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing.Datascope Corp. recalls Cardiosave Hybrid. Intra-Aortic Balloon Pump system. and 1 more products
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.Medline Industries, LP recalls CURAD Germ-Shield Touch-Free Fabric Bandages and 6 more products
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the…Fagron Compounding Services recalls Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic…
Incorrect Product FormulationGlenmark Pharmaceuticals Inc., USA recalls Nebivolol Tablets
Cross Contamination with Other ProductsCipla USA, Inc. recalls Cinacalcet Hydrochloride Tablets and 2 more products
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.Lupin Pharmaceuticals Inc. recalls Sertraline Hydrochloride Tablets USP
Defective container - seal not adhering to bottlesLupin Pharmaceuticals Inc. recalls Ganirelix Acetate Injection
Failed impurities/degradation specifications: out of specification results for Ganirelix acetate acrylic acid adduct impurity.Winder Laboratories, LLC recalls Morphine Sulfate Oral Solution 100 mg / 5 mL
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.Dr. Reddy's Laboratories, Inc. recalls Varenicline Tablets
Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.Cipla USA, Inc. recalls Lanthanum Carbonate chewable tablets and 1 more products
Failed stability specifications: Out of specification for hardness test
CanadaUniCel DxI 600 and 800 Access Immunoassay Systems
Beckman Coulter UniCel DxI 600 and 800 instruments fail to start after rebooting because the AuObj.exe software does not launch.Firstar® CPR Face Shield
Identified as unauthorized/misreppresented/counterfeit by the manufacturer.
Wyld Canna Inc d.b.a Wyld Canna recalls Real Fruit Mixed Berry CBD Gummies due to packaging and labelling issue
The affected products are packaged in the wrong pack.A little guidance
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