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 23 minutes ago
United StatesCardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays… and 11 more products
The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process.Diagnostica Stago, Inc. recalls STA Staclot Protein S
A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identifiedAVID Medical, Inc. recalls Halyard medical convenience kits labeled as: 1) ENT and 2 more products
The recall notice was initiated due to a Medicom Urgent Medical Device Recall.Medline Industries, LP recalls Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT and 15 more products
The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper…Golden State Medical Supply Inc. recalls Prasugrel HCI
Failed Dissolution Specifications.Mylan Pharmaceuticals Inc recalls Carton label: Mycophenolate Mofetil for injection
Failed Dissolution SpecificationsMylan Pharmaceuticals Inc recalls Prasugrel Tablets
Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteriaChiesi USA, Inc. recalls Revcovi
Failed Stability Specifications: Out of specification stability result for the protein concentration profile.Sage Products, LLC recalls 2% Chlorhexidine Gluconate* Cloth
Cross Contamination with Other ProductsBionpharma Inc. recalls Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg
Presence of Foreign Tablets/CapsulesLexia LLC recalls Broadway Joe's Pain Cream and 1 more products
CGMP Deviations: Potential contamination of raw materialAllies Group Inc. recalls THE ONE SPF 50 INVISIBLE SUNSCREEN GEL and 3 more products
Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 500 mL
Presence of particulate matter: Particulates identified as fiberglassTeva Pharmaceuticals USA, Inc recalls traZODone Hydrochloride Tablets
Presence of Foreign Tablets/CapsulesAmerican Health Packaging recalls Buprenorphine Sublingual Tablets
Labeling: Label Mix-upSupernus Pharmaceuticals, Inc. recalls Trokendi XR
Failed dissolution specifications.Optimal Balance Pharmacy recalls Glutathione 200 mg/mL
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.Baxter Healthcare Corporation recalls Vancomycin Injection and 16 more products
CGMP Deviations
BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect
The firmware version, G3-2.00.76 installed on the Luna G3 APAP (Model LG3600) devices contained a firmware defectPhilips 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.A little guidance
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