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 9 minutes ago
United StatesBoston Scientific Corporation recalls FARASTAR Ablation Generator EU
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter.Boston Scientific Corporation recalls FARADRIVE Steerable Sheath Clear IDE and 3 more products
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator…JB Chemicals and Pharmaceuticals Ltd recalls Cetirizine Hydrochloride Tablets USP 5 mg
Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets USP 5 mg.Rising Pharma Holding, Inc. recalls Rising
Presence of Precipitate: medication was crystallizing and particles floating in the bottlePrecision Dose Inc. recalls Glycopyrrolate Oral Solution
Failed Impurities/Degradation SpecificationsAscend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets
Failed Dissolution Specifications; Olmesartan Medoxomil content below specificationsAsclemed USA Inc. recalls Lidolog Kit
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scanBionpharma Inc. recalls Divalproex Sodium Delayed-Release Tablets
Presence of Foreign Tablets/CapsulesAscend Laboratories, LLC recalls Dabigatran etexilate Capsules and 1 more products
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total…Fresenius Kabi USA, LLC recalls Glycopyrrolate Injection and 4 more products
Presence of Particulate Matter: Hair was found in product Presence of Particulate Matter: Hair was found in productsSupernus Pharmaceuticals, Inc. recalls Trokendi XR
Failed Dissolution SpecificationsMajor Pharmaceuticals recalls Levothyroxine Sodium Tablets and 11 more products
Subpotent DrugRohto-Mentholatum (Vietnam) Co., Ltd. recalls Rohto Cooling Eye Drops ALL-IN-ONE and 7 more products
Lack of Assurance of Sterility3B Medical, Inc. recalls Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number…
Packaging and labeling discrepancy involving product size identification and associated Unique Device Identifier (UDI/GTIN).Intuitive Surgical, Inc. recalls da Vinci SP Instrument Arm Drape
Robotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the product, which may…Maquet Cardiovascular, LLC recalls The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System
Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run…Medtronic Perfusion Systems recalls Medtronic DLP One-Piece Pediatric Arterial Cannula and 1 more products
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.Medline Industries, LP recalls Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267 and 1 more products
Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach.Tosoh Bioscience Inc recalls ST AIA-Pack Testosterone
The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could cause…Argon Medical Devices, Inc recalls Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F and 5 more products
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.Oscor Inc. recalls Abiomed REF: 0052-3025 and 2 more products
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines…Olympus Corporation of the Americas recalls Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188. and 3 more products
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the…GE Medical Systems, LLC recalls Optima XR200amx and 2 more products
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may…A little guidance
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