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 2 minutes ago
United StatesGreenwich Rx recalls Glutathione Injection
Microbial Contamination of Sterile ProductsViatris, Inc. recalls Telmisartan and Amlodipine
Superpotent Drug: potential for the Telmisartan content in these lots to exceed specificationsShenzhen Techdow Pharmaceutical Co., Ltd. recalls Heparin Sodium Injection
Lack of Assurance of SterilityHikma Pharmaceuticals USA INC. recalls Abirtega
Failed Tablet/Capsule Specifications: Failed tablet specifications for weight uniformity.Strides Pharma Inc recalls Cinacalcet Tablets
Failed dissolution specificationsPar Health USA, LLC recalls Argatroban Injection and 1 more products
Particulate matter: particulate matter identified as cellulose, polystyrene, polyethylene teraphalate, stainless steel, or stopper material in the product solution.Pritam International Private Limited recalls Brush Buddies and 16 more products
CGMP Deviations CGMP Deviations.
Tonight We Ride, LLC Issues Voluntary Recall of Ultimate Forza Male Supplement Due to Presence of Undeclared Sildenafil, Tadalafil, and Dapoxetine
Product contains undeclared Sildenafil, Tadalafil, and DapoxetineNeuronetics, Inc. recalls NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number…
Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly.Boston Scientific Corporation recalls NaviFlex LW Pusher
Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device…Merit Medical Systems, Inc. recalls Scout MD
The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.Healthmark Industries Co., Inc. recalls Vinyl Instrument Guards
Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated.Becton Dickinson & Co. recalls BD Phoenix Panel NMIC-312. Catalog Number: 449082. and 1 more products
Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.Sarnova HC, Llc recalls Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack
Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.Integrated Medcraft LLC recalls FORWARD Gunshot Wound Kit
Subrecall of a kitted device from SafeGuard Medical due to internal testing identified an issue affecting the device's sterile pad, potentially causing the sterile pad…Ethicon, LLC recalls PERMA-HAND Silk Black Braided Sterile Nonabsorbable Surgical Suture
Silk sutures, indicated for use in cardiovascular, ophthalmic and neurological procedures, packaged with alcohol-based fluid, not part of product design, that if…W L Gore & Associates, Inc. recalls Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis
The potential for the devices to be mislabeled with the incorrect length.Microgenics Corporation recalls MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control
Vial-to-vial variability in MAS¿ Omni"IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, Lot OPRO29061A results in low Parathyroid Hormone (PTH)…Steris Corporation recalls RAPICIDE PA Part A High-Level Disinfectant and 2 more products
If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure.Jenavalve Technology Inc. recalls JenaValve Trilogy Delivery Catheter and 2 more products
Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device.In2bones USA, LLC recalls REF: P65 ST862 CoLag SCREW
Due to labeling error, bone screws specified as fully threaded, are actually partially threaded screws.SI-BONE, Inc. recalls iFuse TORQ Implant System Model/Catalog Number: 10055T
The pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be ensured.Cadwell Industries Inc recalls Brand Name: IOMAX Product Name: IOMAX Cortical Module Model/Catalog Number: 190296-200…
Stimulator device contains a defective printed circuit board assembly (PCBA) that may cause the device to unintentionally deliver electrical stimulation to the patient…A little guidance
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