Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 3 minutes ago
United StatesMicroPort Orthopedics Inc. recalls Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog…
Due to products not having FDA Premarket authorization to be distributed within the United States.Baxter Healthcare Corporation recalls SIGMA Spectrum Infusion Pump
Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears.Leaseir Technologies Slu recalls Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b…
The console label for affected devices is missing the "DANGER" symbol.Tyber Medical recalls Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate… and 1 more products
The supplier manufactured anatomical left plates with an incorrect thread orientation.Community Products, LLC recalls Rifton Equipment and 2 more products
Potential for fraying on the body support strap.Ge Medical Systems Israel, Functional Imaging recalls GE Healthcare Omni Legend
There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images.ICU Medical, Inc. recalls Tego Connector: REF: 011-D1000
Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may…ICU Medical, Inc. recalls ICU Medical Plum Duo Infusion Pump and 2 more products
Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy.Medline Industries, LP recalls MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed and 5 more products
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires.Merit Medical Systems, Inc. recalls Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers… and 6 more products
Inflation device handle may detach from the syringe during procedure.Philips Medical Systems Nederland B.V. recalls Philips Azurion system
Philips has identified two (2) software issues affecting device systems that may result in loss of imaging (X-ray) functionality and/or loss of motorized movement…Edan Diagnostics recalls Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2 and 15 more products
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.Raysearch Laboratories Ab recalls RayStation/RayPlan. Model/Catalog Number: 10.1. Software Version: RayStation/RayPlan… and 8 more products
Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs).Specialty Process Labs LLC recalls Thyroid
Subpotent DrugGraviti Pharmaceuticals Private Limited recalls Furosemide Tablets
Presence of Foreign SubstanceZydus Pharmaceuticals (USA) Inc recalls Icosapent Ethyl capsules
Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsulesCipla USA, Inc. recalls Diclofenac Sodium Topical Gel
Failed PH Specifications
United KingdomPilgrim Anti-Dandruff Shampoo and Conditioner Set sold via Amazon safety warning
The product presents a serious chemical risk as the ingredients list indicates it contains Zinc Pyrithione, which is prohibited for use in cosmetic products.
CanadaCleverCut and FlowCut Sphincterotomes
CleverCut and FlowCut sphincterotome devices which did not undergo thermoforming could deform and lose performance.MOLLI 2 Systems
Stryker has updated the MOLLI 2 system Instructions for Use (IFU) following two medical device reports (MDRs) submitted to the FDA (June 5 2025).Bard Marquee 12g X 10 cm
In September 2024, BD initiated a field action for specific lots of the Marquee™ Disposable Core Biopsy Instruments that were potentially manufactured missing the…OES Pro Urology Resection Sheaths
Further to the FY25-022 medical device recall issued in October 2024, Olympus is informing users of a voluntary product recall action for cystoscope outer sheath.Thinking about buying GLP-1 drugs like Ozempic or Mounjaro? Beware of fake or unauthorized products
With growing interest in GLP-1 products such as semaglutide (e.g.A little guidance
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