Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 4 minutes ago
United StatesConvaTec, Inc recalls Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in.
Surgical dressing manufactured out of specification (greater thickness).QuVa Pharma, Inc. recalls Methohexital Sodium
Failed Impurities/Degradation SpecificationsBioMed Laboratories, LLC. recalls Medline Remedy Specialized Silicone Cream
Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.Reliance Life Sciences Private Limited recalls Pemetrexed for Injection 100mg/Vial and 3 more products
Lack of Sterility AssuranceShimoga Chemicals recalls Clomiphene Citrate USP Active Pharmaceutical Ingredient
cGMP deviationsGasco Industrial Corp. recalls Gasco Isopropyl Alcohol 70% and 5 more products
Subpotent drugOnesource Specialty Pharma Limited recalls Methohexital Sodium for Injection
Failed Impurities/Degradation Specifications
CanadaBD ChloraPrepâ„¢ Clear - 1mL Applicator: Product sterility
Product sterility could be compromised in affected lots.Oribe Serene Scalp Densifying Shampoo; Presence of bacterial contamination
Affected lots may contain the presence of bacterial contamination (pluralibacter gergoviae).Apo-Tiotropium Capsules; Out-of-specification (particle size)
The particle size did not meet the specifications in the affected lots.Phantom® Hindfoot TTC/TC Ball Tipped Guide Rod
Zimmer Biomet Canada on behalf of Paragon 28, Inc.Astral 150â„¢
An internal electrical component (supercapacitor) may leak electrolyte over time.Mequ A/S ºM Warmer Leakage
A misplaced seal may cause leakage internally in the ºM Warmer device.
United KingdomPr. Francoise Bedon Paris Carotte Lightening Body Lotion safety warning
The product presents a serious chemical risk as according to the list of ingredients, it contains hydroquinone (1,4-dihydroxybenzene).
Two lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges
Sandoz Canada Inc.Alice Le System - Sleepware Software
Philips Respironics has become aware of a compliance issue with Sleepware G3 versions 4.0.0.0 and above, where the original 4.0 update was not licensed appropriately in…Allura Xper FD10
Philips has identified through customer complaints that, during certain repair or service actions, Hard Disk Drives (HDD) with different performance characteristics…Hamilton Medical AG recalls IntelliCuff
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error.BD Switzerland Sarl recalls MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461…
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S.Medacta Usa Inc recalls Short Monobloc Stem Broaches
Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem…Laborie Medical Technologies Corp recalls Solar GI System
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing…Medline Industries, LP recalls Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH
Expansion of RES 98277.Medtronic Heart Valves Division recalls Medtronic Harmony Delivery Catheter System
Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system under…A little guidance
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