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 4 minutes ago
United StatesAccord Healthcare, Inc. recalls Levothyroxine Sodium Tablets
Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.RC Outsourcing, LLC recalls Bevacizumab 1.75 mg/0.07 mL
Lack of assurance of sterility.Acuity Specialty Products, Inc. recalls Wyandotte and 1 more products
cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand sanitizers was not…Acella Pharmaceuticals, LLC recalls Doxycycline Hyclate Tablets
Failed dissolution specifications: Stability testing found that the lot did not meet dissolution specifications.The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recalls Major ChlorproMAZINE Hydrochloride Tablets and 4 more products
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limitAvKARE recalls Norgestimate and Ethinyl Estradiol Tablets
Failed Content Uniformity SpecificationsGenoGenix LLC recalls Alpha Lipoic Acid for Injection and 56 more products
Lack of Assurance of Sterility Microbial Contamination of Sterile Products: elevated endotoxin levelsW L Gore & Associates, Inc. recalls GORE ACUSEAL Vascular Graft
Reports of vascular graft delamination, which may lead to reduced access flow; cannulation difficulties; bleeding or bruising; and harms related to reintervention…Bard Peripheral Vascular Inc recalls Venclose digiRF Generators
Software version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring anomalies in…S.I.N. Implant System Ltda recalls IMPLANT EPIKUT PLUS MT16 3
Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging…Beckman Coulter Inc. recalls DxC 500 AU Module w/ISE
On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the…bioMerieux, Inc. recalls VITEK¿ 2 Gram-negative AST Test Kits
Potential for false resistant results for Colistin (cs02n) with multi-drug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii complex used in specific cardsLeMaitre Vascular, Inc. recalls Artegraft Collagen Vascular Grafts Model Numbers:
The bovine carotid arteries used to produce the impacted grafts from affected lots were sourced using raw material from a supplier that had not been reviewed and…Medline Industries, LP recalls Medline Kits: 1) VALVE PACK-LF
The kits contain certain lots of cannula products where the catheter may not retain its shape.Change Healthcare Canada Company recalls Change Healthcare Radiology Solutions software version 14.2.2
Due to software issue, radiology reports may not be fully displayed when viewing.Howmedica Osteonics Corp. recalls 1. EXETER V40 STEM 44MM NO 2
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa.Medline Industries, LP recalls Sterile Medline Convenience Kits: 1) MAJOR PACK L-F and 1 more products
Convenience kits labeled as sterile have not gone through the sterilization process.Schiller, Ag recalls Argus PB-3000
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the…Getinge Disinfection Ab recalls Getinge 88-Series Washer- Disinfector. Model Number: 88-5.
Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure…Aesculap AG recalls AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R. and 1 more products
Mislabeling.Philips Medical Systems Nederland B.V. recalls Allura Xper FD10C and 14 more products
The BIOS battery may deplete faster than initially anticipated during the design phase.Medline Industries, LP recalls Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH… and 4 more products
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates.Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software… and 1 more products
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.A little guidance
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