Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,302 recalls, newest first · Checked 1 minute ago
United StatesAjanta Pharma USA Inc recalls Ranolazine Extended-Release Tablets
Failed Dissolution Specifications: below specificationPar Health USA, LLC recalls Buprenorphine Hydrochloride
CrystallizationApotex Corp. recalls Paroxetine Extended-Release Tablets
Failed dissolution specifications.Aurobindo Pharma USA Inc recalls amazon
Discoloration: consumer complaints received for discolored tabletsTerSera Therapeutics LLC recalls Zoladex
Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.Aurolab Trust recalls FOCUS PI Hypromellose 0.7% Formula
Lack of Assurance of SterilityAmneal Pharmaceuticals, LLC recalls Estradiol Gel
Defective Container; packets were found to be either empty or partially full.SV Labs Toronto Corporation recalls Benzoyl Peroxide Wash and 1 more products
Microbial contamination of topical product.
CanadaPerma-Sharp Sutures
Perma-sharp sutures are manufactured for Hu-Friedy by 2 manufacturers.Pacific Health Sciences Voluntarily Recalls One Lot of Babies' Magic Tea Brand Baby Sleep Gripe Water Dietary Supplement
Product contains undeclared ethanol, methanol, and isopropanol
Leader Formulas, LLC. Issues Voluntary Nationwide Recall of RAPTURE Preworkout Due to the Presence of 1,3-Dimethylamylamine (DMAA)
Product contains 1,3-Dimethylamylamine (DMAA)Fluoroplastic Vent Tube
Vent tube devices across lot 0231048280 were identified to have been released to customers without undergoing sterilization.Cardinal Health General Procedure Tray
Cardinal Health was recently informed of a medical device recall from Becton Dickinson concerning the BD Alaris™ Pump Infusion sets used with BD Alaris™ pump module…Embletta MPR PG
Natus has become aware of complaints related to certain Embletta MPR devices where the device is unable to correctly format its internal memory.FreeO2 Automated Oxygen Therapy Device Adult & Pediatric
A battery reading error may occur when certain Freeo2 HW 1.2 devices are restarted following an upgrade from software version 1.2.X to 1.4.X.Medline Bariatric Rollator
Specific lots of Medline BariatricRollator (SKU: MDS86800XWS), are being recalled due to the front fork stem bolt/wheel assembly disconnecting from the rollator frame…
CzechiaPJMASKS cosmetics set safety alert: chemical risk
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is prohibited in cosmetic products.
GermanyLong 4 Lashes eyelash serum safety alert: chemical risk
Chemical analysis of the sample in question detected a level of 0.026 g/100 g (equivalent to 263 μg/g) of bimatoprost methyl amide (Methylamido-Dihydro-Noralfaprostal…Nova Biomedical® Announces Global Medical Device Correction for StatStrip® Glucose Hospital Meter
Software issue may cause a glucose result to be associated to the wrong patientLumify Ultrasound System
Potential issues with the Lumify Diagnostic Ultrasound System which may prevent or delay scanning functionality: Due to a software issue, the Lumify application may not…Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.PDP-DIPHENHYDRAMINE 25 MG CAPSULE: Out-of-specification (Impurity)
The impurity, N-Nitroso-N-Desmethyl Diphenhydramine, is out of specification in the affected lots.Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.A little guidance
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