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 2 minutes ago
United StatesUnited Orthopedic Corp. recalls Brand Name: U2 Total Knee System Product Name: PSA Box Trial and 3 more products
Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.Siemens Healthcare Diagnostics, Inc. recalls Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls SMN 10445390 Catalog…
out-of-specification sodium azide concentration in Syva Emit Tox Serum Tricyclic Antidepressant Calibrator/Controls Lot U2.Zydus Pharmaceuticals (USA) Inc recalls Mirabegron Extended-Release Tablets
CGMP: Due to Out of Specification (OOS) result for N-Nitroso Mirabegron impurity.Central Admixture Pharmacy Services Inc recalls Total Parental Nutrition
Incorrect Product FormulationSunny Pharmtech Inc. recalls Cyclophosphamide for Injection and 1 more products
Presence of Particulate Matter; identified as stainless steelAurobindo Pharma USA Inc recalls Dicyclomine Hydrochloride Capsules
shortfill; reports of empty capsules.Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be…Permobil Inc recalls M5 Corpus Power Wheelchair REF
This recall is being reported retroactively.Permobil Inc recalls Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031
This recall has been reported retroactively.Argon Medical Devices, Inc recalls L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga and 1 more products
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may…Philips Medical Systems recalls Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000… and 2 more products
The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually.Terex Utilities recalls Power Over Fiber Base Module
Device not certified - no laser product report was filed with CDRH prior to distribution.IsoTis OrthoBiologics, Inc. recalls OsteoBallast
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with…Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack and 3 more products
The recall notice was initiated due to a Medicom Urgent Medical Device Recall.ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides…
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of…Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR and 5 more products
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass.Stryker GmbH recalls Stryker Hoffmann II Connecting Rod Micro 3 x 30mm. Catalog Number: 50796030. and 6 more products
Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.Instrumentation Laboratory recalls GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with… and 2 more products
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: SPINAL KIT and 7 more products
Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP.Micro Labs USA Inc recalls Dorzolamide HCl and Timolol Maleate Ophthalmic Solution
Defective Container: Firm received multiple complaints of broken cap spikes and undeliverable drops.Mylan Pharmaceuticals Inc recalls Mycophenolate Mofetil for Injection USP
Presence of precipitateGlenmark Pharmaceuticals Inc., USA recalls Azelaic Acid Gel
CGMP Deviations: Product quality complaints concerning abnormal texture or consistency (described as grainy, gritty, or sandy) were received.Ascend Laboratories, LLC recalls Dabigatran Etexilate Capsules and 2 more products
Failed impurity/degradation specification: an OOS result observed in Related substance test analysis w.r.t Impurity II, Impurity III and Total impurities for 12-month…A little guidance
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