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 11 minutes ago
United StatesOlympus Corporation of the Americas recalls Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and… and 19 more products
Complaints of the ceramic tip of the resection sheath breaking have been received.Medline Industries, LP recalls Medline Kits containing Tego Connectors: Medline IR Pack and 5 more products
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits.Agebox recalls Agebox iKids-Growth and 1 more products
Marketed Without an Approved NDA/ANDA: presence of undeclared ibutamorenLeo Pharma Inc recalls Adbry
Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.AvKARE recalls Amantadine HCl
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.Slate Run Pharmaceuticals recalls Eptifibatide Injection
Labeling: Not Elsewhere Classified.Wizcure Pharmaa Private Limited recalls Vista Tears Polyethylene Glycol 400 0.4% w/v and 6 more products
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.Centinel Spine, Inc. recalls Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software…
Products were mislabeled as the 6mm product but included the 5 mm product.Intuitive Surgical, Inc. recalls Da Vinci 5 ASSY
An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower…Medica Corporation recalls Medica Capillary Tubes
A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica…Stryker Corporation recalls MOLLI 2 System System includes: MM1000
Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue…Baxter Healthcare Corporation recalls Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009…
Pumps were released without full testing being performed, including occlusion alarm testing.Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the… and 2 more products
Issue with software algorithm which may lead to overpressure events.Auris Health, Inc recalls MONARCH Platform
Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading…Wilson-Cook Medical Inc. recalls Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code…
Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during…Medline Industries, LP recalls Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets…Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm and 11 more products
Firm is initiating a removal due to continued reports of adverse events.Integra LifeSciences Corp. (NeuroSciences) recalls MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: and 2 more products
Potential packaging failures, which could lead to a breach in the sterile barrier.Bard Peripheral Vascular Inc recalls Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff…
Due to damage to outer tray that can potentially compromise the sterile barrierImmunotech A.S. recalls Estrone RIA
The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability.Medline Industries, LP recalls Medline Convenience Kits: 1) ANCILLARY PACK-LF and 41 more products
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices.Hologic, Inc recalls Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.
Presence of particulates in affected devices that can be deposited into breast tissue during use.Steris Corporation recalls Barco MNA with the HexaVue IP Integration System
This is a sub-recall of event RES 96885.A little guidance
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