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 1 minute ago
United StatesBaxter 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 SpecificationsC-Rad Positioning Ab recalls Brand Name: Catalyst+ Product Name: Catalyst
Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups.Boston Scientific Corporation recalls Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter
Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter…Medtronic Inc recalls Abre Venous Self-Expanding Stent System
Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force.ICU Medical, Inc. recalls Plum Duo Infusion System
ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound.Thoratec LLC recalls CentriMag Blood Pump
Acute circulatory support system pump may not fit into the motor and reports received of the pump not being securely locked into the motor using the screw-in locking…Instrumentation Laboratory recalls The product is used for the evaluation of the intrinsic coagulation pathway
Potential for microbial contamination.Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Emphasizing instructions for LVP duration programming located in the IFU.A little guidance
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