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 StatesBreckenridge Pharmaceutical, Inc. recalls Duloxetine Delayed-Release Capsules
CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment limit of 12.5ppm.QuVa Pharma, Inc. recalls R.E.C.K.
Presence of Particulate MatterAcme United Corporation recalls Sting Relief Swabs
Product Mix-upOtsuka ICU Medical LLC recalls 0.9% SODIUM CHLORIDE Injection
Lack of Assurance of Sterility: Potential for flexible container leaks.Amerisource Health Services LLC recalls Prazosin Hydrochloride and 2 more products
Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake…Kenvue Brands LLC recalls TYLENOL
Defective ContainerSamsung Bioepis Co., Ltd. recalls HADLIMA
Lack of Assurance of Sterility.Endo USA, Inc. recalls Everolimus tablets 5mg and 3 more products
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.Letco Medical LLC recalls Espumil
Labeling: Not Elsewhere ClassifiedHeritage Pharmaceuticals Inc recalls Desipramine Hydrochloride Tablets and 5 more products
CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.Sun Pharmaceutical Industries Inc recalls Lisdexamfetamine Dimesylate Capsules and 6 more products
Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH)…Teva Pharmaceuticals USA, Inc recalls Prazosin Hydrochloride and 2 more products
CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the…Farmakeio Outsourcing LLC recalls Testosterone 25MG and 14 more products
CGMP Deviations: Potential presence of metal particulate matterProRx LLC recalls Semaglutide Injection and 6 more products
Lack of Assurance of SterilityHome Health US, Incorporated recalls One Step Sterile Lancet for Single Use
Due to incorrect/lack of Unique Device Identifier (UDI) codes.HeartSine Technologies Ltd recalls HeartSine Pad-Pak
Due to customer complaints, defibrillator pads may contain damage pins that disrupt the mechanical fit and electrical contact.Biomet, Inc. recalls BIOMET ZipTight
There is a potential for a missing slotted button assembly in one lot of ZipTight, Acute AC Joint Implant, Single ZiploopLeMaitre Vascular, Inc. recalls Artegraft¿ Collagen Vascular Graft
The device was incorrectly packed in the wrong size labeled outer packaging.B Braun Medical Inc recalls Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET FOR DIALOG…
The potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.Beckman Coulter, Inc. recalls DxC 500i Clinical Analyzer Modules and 1 more products
Beckman Coulter has confirmed a software anomaly on DxI 9000 Access Immunoassay Analyzer and the DxC 500i Clinical Analyzer that may prevent correct application of…Abiomed, Inc. recalls Automated Impella Controller
Potential for Automated Impella Controller (AIC) purge pressure issues due to purge retainer failures.GE Medical Systems, LLC recalls MAC VU360 Acquisition Trunk Cable and Module Holder
If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the Acquisition Trunk Cable.Synthes (USA) Products LLC recalls LOW PROF LCKNG SCREW and 1 more products
Although the etched length on the screw is correct, the length marked on the external packaging is incorrect.A little guidance
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