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 StatesPhilips Medical Systems Nederland B.V. recalls Allura Xper FD. Model Numbers: 722026
Firmware issue potentially leading to loss of geometry movements.Medline Industries, LP recalls Medline Micro-Kill Bleach Germicidal Bleach Wipes and 3 more products
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month…Microvention Inc. recalls BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US…
Due to an increase rate of balloon pinhole defects.Covidien, LP recalls V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22… and 4 more products
Product may contain a perforation or tear in the sterile barrier packaging.Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) FAT GRAFT ADD KIT and 7 more products
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.W L Gore & Associates, Inc. recalls GORE VIABIL Short Wire Biliary Endoprosthesis and 1 more products
10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes…Baxter Healthcare Corporation recalls Cefazolin in Dextrose
Presence of Particulate MatterNovartis Pharmaceuticals Corporation recalls Diovan
Failed Dissolution SpecificationsPrestige Brands Holdings recalls CLEAR EYES Maximum Itchy Eye Relief
Lack of assurance of sterility.Heritage Pharmaceuticals Inc recalls CLINDAMYCIN PALMITATE HYDROCHLORIDE FOR ORAL SOLUTION
Presence of Foreign Substance: presence of particles and white flakes in the reconstituted bottles.Liebel-Flarsheim Company LLC recalls Optiray Imaging Bulk Package-350
Presence of Particulate Matter: comprising polyethylene and other plastic materials, stainless steel and glass.Victory Medical Center Pharmacy recalls Glutathione
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.Apollo Care, LLC recalls SEMAGLUTIDE 12.5MG and 10 more products
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type materialShoolin Pharma Chem LLP recalls SILDENAFIL CITRATE USP and 4 more products
CGMP Deviations:Noted during FDA inspectionBuy-Herbal recalls Kian Pee Wan Capsules
Marketed Without an Approved NDA/ANDA: Product contains undeclared drug ingredients dexamethasone and cyproheptadine.Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i…
Events observed where anesthetic agent was not delivered when the vaporizer was activated.Siemens Healthcare Diagnostics, Inc. recalls Syva Emit Disopyramide Assay Enzyme Immunoassay
Out-of-specification sodium azide concentration in Syva Emit Disopyramide Enzyme Immunoassay Calibrator Lot U1.Contego Medical, Inc recalls Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated…
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter, that due to a wire-to-filter-bond issue, may fail to…Philips Medical Systems Nederland B.V. recalls Philips Allura under the following System Descriptions and corresponding model numbers… and 2 more products
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.Nuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument…
Due to a software issue which may result in false co-infection (e.g., Positive for Flu A, when SARS-CoV-2 is present).Therabody, Inc recalls Charger for the Therabody Theragun
Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire).Beckman Coulter Biomedical GmbH recalls REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info…
Due to software issues where does not handle combo assay results.Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence…
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.A little guidance
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