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 8 minutes ago
United StatesAbiomed, Inc. recalls Impella CP Set with SmartAssist. Product Codes: 1000080
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory…Arrow International, LLC recalls PARACENTESIS KIT and 34 more products
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets.Inspire Medical Systems Inc. recalls Brand Name: Inspire Medical Systems and 1 more products
Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer.Medtronic Navigation, Inc.-Boxborough recalls Medtronic O-arm O2 Imaging System. Model Number: BI70002000.
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.Medline Industries, LP recalls MEDLINE Urethral Catheter and 29 more products
During an internal review, Medline identified representative samples did not meet applicable performance specifications.Par Health USA, LLC recalls Buprenorphine HCl
Crystallization; identified as Buprenorphine free baseGlenmark Pharmaceuticals Inc., USA recalls Alyacen 7/7/7
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.Sandoz Inc recalls Focalin XR
Labeling: Incorrect or Missing Lot and/or Exp DateAjanta Pharma USA Inc recalls Aripiprazole Tablets USP
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.PAI Holdings LLC recalls VistaPharm and 3 more products
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023Inventia Healthcare Limited recalls Chlorthalidone Tablets
Failed Dissolution SpecificationsIntegraDose Compounding Services LLC recalls Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride
Subpotent DrugDabur India Limited recalls Lucky Super Soft and 13 more products
CGMP Deviations; deficiencies observed during FDA inspectionKeystone Industries recalls Pearson Quality Topical Anesthetic Gel and 6 more products
Defective container:may contain bottles with incomplete sealsBerlin Heart GMBH recalls EXCOR Pediatric Ventricular Assist Device
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.Abbott Medical recalls Merlin" Patient Care System
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.Medartis AG recalls Medartis APTUS
The cannulation of the CCS screw is not centered.Inter-Med Llc recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit
Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel.DT MedTech, LLC recalls Hintermann Series Talar Implant
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.Boston Scientific Corporation recalls Orca Single Use Air/Water and Suction Valves
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the…Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic…Fresenius Medical Care Holdings, Inc. recalls Bicarby" Dialysate
Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of…ICU Medical, Inc. recalls Plum Solo Precision IV Pump and 2 more products
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting…A little guidance
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