Go Back to Shop
All CategoriesAbout PlannersAnimals and PetsBathroomBeauty EssentialsFor ChildrenFor MenFor WomenGadget EssentialsGardeningHelping HandKitchen EssentialsNewsRelaxationSports
FDA announces Class I recall of iCast stent
by
FDA announces Class I recall of iCast stent
hnesich_drupal
Jun 2, 2022
Atrium Medical Corporation has recalled the iCast Covered Stent System due to reports of separation of the balloon or catheter hub separation when removed from the patient, potentially causing serious patient harm, the Food and Drug Administration announced today. Health care providers should read and follow the Urgent Medical Device Correction letter and report any product performance issues to Atrium Medical Corporation, FDA said. A Class I recall is the most serious type of recall.
Headline
Leave a comment
You must be logged in to post a comment.