Medical Device Recalls | FDA - U.S. Food and Drug Administration
Summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could cause serious health problems or...
Air Compressor Device Correction: GE HealthCare Provides …
Oct 29, 2024 · This recall involves updating recall instructions for using these devices, and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most ...
Insulin Pump Recall: Medtronic Notifies Users of MiniMed 600 …
Oct 17, 2024 · Medical Device Recall Database Class 1 Device Recall MiniMed 620G, 630G (OUS only), 640G, and 740 Insulin Pumps. (fda.gov) Class 1 Device Recall Medtronic MiniMed 630G and 700G Insulin Pumps (fda ...
Medical Device Recalls - Food and Drug Administration
4 days ago · This database contains Medical Device Recalls classified since November 2002. Since January 2017, it may also include correction or removal actions initiated by a firm prior to review by the...
Medical Device Recalls - Food and Drug Administration
Nov 8, 2024 · This database contains the classified Medical Device Recalls since november 1, 2002. to search, enter a single word (e.g., electromechanical), an exact phrase (e.g., electromechanical pump) or...
Tracheostomy Tube Recall: Smiths Medical Removes BLUselect, …
Oct 25, 2024 · Medical Device Recall Database Smiths Medical portex BLUperc Percutaneous Diliation Procedural Trays with BLUselect tracheostomy tubes Smiths Medical portex BLUselect, tracheostomy tube
Medical Device Recalls News - MedTech Dive
Oct 21, 2024 · Medical device safety in spotlight after high profile recalls. From Philips’ massive recall of respiratory devices to ongoing health risks with breast implants, medical devices tied to patient harm have put a focus on product safety. By MedTech Dive staff
Medical Device Recall Information - Philips Respironics Sleep …
In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).
Consumer Safety Alert: CPSC Issues Urgent Warning About Adult …
1 day ago · Adult portable bed rails are an important device used in assisted or residential care settings and private homes to help prevent falls or injuries for individuals with physical or mental limitations. ... Essential Medical Supply Recalls Adult Portable Bed Rails Due to Entrapment and Asphyxia Hazard; One Death Reported. Compass Health ...
Device Recalls - Food and Drug Administration
A recall is an action taken to address a problem with a medical device that violates FDA law. Recalls occur when a medical device is defective, when it could be a risk...