Medical Device Network on MSN10d
FDA tags Medtronic embolisation device recall as Class I
The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...
This Very Popular Laundry Detergent Has Been RECALLED Over Bacteria Concerns
Woolite Delicates laundry detergent units were recalled due to potential bacterial contamination with Pseudomonas. Here’s a ...
Medical Device Network on MSN8d
FDA tags Becton, Dickinson and Company infusion software recall as Class I
Problematic software has been the cause of multiple infusion pump recalls in the medical device industry over the past few ...
MassDevice10d
Medtronic recalls embolization device after reported deaths
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
Medtronic recalls aneurysm-treating device linked to four deaths
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
health.economictimes.indiatimes9d
FDA classifies recall of Medtronic embolization devices as 'most serious'
Bengaluru: The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", following reports of the deaths of four patients. The use of ...
MassDevice7d
Smiths Medical has a serious recall involving vein access ports
The FDA has labeled Smiths Medical's recall of ProPort Implantable Plastic Port as Class I, the most serious kind.
Insurance Business America12d
Australian product recalls climb amid regulatory changes – Sedgwick
Product recalls across key Australian industries increased by 14% in the second half of 2024 compared to the first half, ...
Medtronic slips after FDA notice on product recall (update)
Medtronic (MDT) stock turned lower as the FDA announced a most serious type of recall involving its Pipeline Vantage 027 ...
Modern Healthcare10d
FDA deems Medtronic’s Pipeline Vantage recall ‘most serious’
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
Becker's Hospital Review15d
3 medical device recalls and corrections
Here are some of the latest recalls reported to the FDA: Olympus recalls single-use guide sheath kits Olympus has recalled certain single-se guide sheath kits due to the risk of the radiopaque ...