Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 1 minute ago
United StatesGranules Pharmaceuticals Inc. recalls Trazodone Hydrochloride
Presence of Foreign Tablets/CapsulesGreen Lumber Holdings, LLC recalls Green Lumber Natural Fuel For Men capsule
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafilUnichem Pharmaceuticals USA Inc. recalls Bisoprolol Fumarate and Hydrochlorothiazide tablets
cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
CanadaAlphenix Systems
An internal error would occur if F-STORE or image acquisition is performed while CAAS clinical analysis function is used.VISERA™ Imaging System
Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of MAJ-210 and MAJ-1218.TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution
Affected lots were manufactured using an active ingredient that was out of specification for dissolution.Cefazolin for Injection: Affected lots are packaged with the incorrect Linear barcode on inner and outer bag labels.
Affected lots are packaged with the incorrect Linear barcode on inner and outer bag labels.MAR-AMLODIPINE: affected lots may contain tablet(s) of Midodrine 2.5mg tablets.
Affected lots may contain tablet(s) of Midodrine 2.5mg tablets.
Two lots of MAR-Amlodipine 5 mg tablets recalled as some bottles may contain the wrong drug
Marcan Pharmaceuticals Inc.UHI-3 High Flow Insufflation System - Insufflator
Olympus is initiating a Medical Device Recall on the High Flow Insufflation Unit Models UHI, UHI-2, UHI-3, and UHI-E.Centricity™ Universal Viewer Zero Footprint Client
Centricity™ Universal Viewer Zero Footprint Client (ZFP) patient timeline may launch incorrect patient.DxC 700 AU and AU5800 Clinical Chemistry Analyzers
Beckman Coulter has determined that some DxC 700 AU and AU5800 Clinical Chemistry Analyzers may unexpectedly generate some errors due to Microsoft® SQL Server® 2022…cobas® pro and cobas® pure
A rare software malfunction has been identified on the cobas® pro (c503) and cobas® pure (c303) platforms affecting the calibration library.CareFusion 303, Inc. recalls BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The BD AlarisTM System…
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital…Elekta, Inc. recalls Brand Name: Elekta Medical Linear Accelerator Product Name: Elekta Synergy
Due to a manufacturing issue and electrical grounding of systems.NIPRO Technical Services, Inc. recalls Conductivity Standard Solution Catalog/Model Numbers: 10001
due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for…LimFlow, Inc. recalls Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Incorrect expiration dateCanon Medical System, USA, INC. recalls Alphenix INFX-8000C and 3 more products
It has been discovered that there is a possibility that the fixing screws of the ceiling movement gear in the ceiling suspended arm that are part of the X-ray…Cerapedics, Inc. recalls PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft
Incorrect expiration dateGold Star Distribution Inc recalls Bandages and first aid kits: FIRST AID KIT 24/42PC and 4 more products
Potential exposure of rodents and rodent activity in the distribution center.Cardinal Health 200, LLC recalls Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal…
The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older.Zimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems… and 1 more products
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings.Miach Orthopaedics recalls BEAR Implant. Model Number: 1000.
Incorrect expiration date on label that extends beyond the product's documented/approved shelf life.A little guidance
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