Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 9 minutes ago
United StatesMedline Industries, LP recalls Medline convenience kits labeled as: 1) FEMORAL PACK and 10 more products
Kits contain a potentially contaminated component which were recalled by the manufacturerApotex Corp. recalls Paxil CR
Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteriaB Braun Medical Inc recalls Lactated Ringer's Injection USP
Presence of Particulate matter.Fresenius Kabi USA, LLC recalls Tyenne
Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.Church & Dwight Co., Inc. recalls Zicam
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testingMallinckrodt Hospital Products Inc. recalls Acthar Gel
Presence of particulate matter: glass and stopper pieceLupin Pharmaceuticals Inc. recalls Clobetasol Propionate Cream USP
Failed content uniformity specifications.Hikma Pharmaceuticals USA INC. recalls Ramipril Capsules USP
Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU).Accord Healthcare, Inc. recalls Levothyroxine Sodium Tablets and 11 more products
Subpotent Drug
CanadaJAMP Temozolomide: Out-of-Specification (Assay)
The active ingredient (temozolomide) is out of specification in the affected lot.Carestation 850
Unexpected shutdown of Carestation 850 and 850C anesthesia systems when AC mains power is disconnected or AC mains power is lost.Semaglutide Injection : Out-of-Specification (Impurity)
An impurity is out of specification in all lots of the affected products.Apo-Semaglutide Injection : Incorrect dose display
The affected lot may display a 2 mg dose in the dose window and deliver a 2 mg dose instead of the expected 0.25 mg or 0.5 mg dose.Automated Impella Controller (AIC)
Abiomed has initiated a voluntary medical device recall (removal) after identification of an increase in complaints related to purge cassette recognition issues due to…Cardinal Health Gynaecology Robotics and Endoscopy Packs
Cardinal Health was recently informed of a medical device recall from Stryker concerning the StrykeFlow PS referenced.pro+ Flat Deck Wide W/O X-Ray
The UDI label for model p7924a13 incorrectly states the product description as "Pro+ 40 MRS surface with x-ray" instead of the actual configuration, which is "Pro+ 36…CARESCAPE Central Station
GE Healthcare has become aware that the CARESCAPE Central Station (CSCS) v3.0.x may not resume patient monitoring for at least 3 minutes following a system restart.BIOFIRE® Joint Infection Panel – 30 Pack
Beginning April 5, 2026, elevated rates of KPC unexpected positives were observed in reagent final QC testing of the BIOFIRE® FILMARRAY® Pneumonia Panel, BIOFIRE®…Med-Rx Medication/Primary Solution Administration Kit
CHS was notified by ICU Medical Canada that they are conducting a recall of certain IV sets as discoloration may be present in the drip chamber of the IV sets.Cyanosure DermaV Laser System
Cynosure Lutronic has identified a adverse trend of complaint reports in North America for spark and loud noise resulting in patient burns during vascular treatment…Maquet Percutaneous Insertion Kit and Dilator Sets
The manufacturer became aware of this issue during retrospective review of historical packaging verification documentation.SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068
Potential for electrical discharge from unit when unplugged.Maquet Critical Care AB recalls GETINGE Y SENSOR Module
The module did not undergo electrical safety tests and functional tests during production.A little guidance
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