Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 22 minutes ago
Otsuka 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 SterilitySistaco Rapid Removal Hub safety warning
The product presents a serious risk of fire because it is fitted with a counterfeit fuse which does not meet the requirements of BS 1362.Rocket® Seldinger Chest Drain Kit
IFU incorrectly states suturing or fixation device to be used.M.Asam VITAMIN C Glow Ampullen 2x14x2ml sold via QVC recall
The product presents a risk of injuries as a small drop of liquid glass material was discovered in the affected batches.Instrumentarium Nagahara chopper
Risk of tip breakage during the cleaning process or during surgery.BK Medical Ultrasound Systems
The instructions for use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures…JODSONE UK Gel Nail Polish Kit sold via Amazon safety warning
The product presents a high risk of electric shock because the plug face does not meet the dimensional requirements of BS 1363.BD Alarisâ„¢ Pump Module
BD was made aware via customer complaints that dropping the BD Alarisâ„¢ Pump Module may cause damage to internal components that may not be apparent or readily visible.Home 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.A little guidance
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