Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 14 minutes ago
United StatesQuVa 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 SpecificationsHamilton 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…Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console.Depuy (Ireland) recalls Depuy Synthes and 1 more products
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.Siemens Medical Solutions USA, Inc recalls ARTIS icono biplane. Model Number: 11327600. and 2 more products
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems… and 1 more products
Potential sterility breach in sealing area of sterile pouch.Windstone Medical Packaging, Inc. recalls A M S and 3 more products
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine…Baxter Healthcare Corporation recalls Adapter for Head Positioning
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the…Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console.Hamilton Medical AG recalls Breathing circuit set
Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which will result…W L Gore & Associates, Inc. recalls GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers
Due to catheter separationMentor Texas LP recalls SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe
A single lot of expired syringes were distributed due to a distribution system control failure.Covidien LLC recalls Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060…
Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.A little guidance
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