The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.

The business, acquired by ICU Medical in 2022, has been dealing with a series of recalls and quality issues over the past ...

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 ...

Over 16,000 bottles of Woolite detergent sold on Amazon have been recalled due to the potential presence of bacteria.

The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the device.

Smiths Medical recalled certain sizes of its Portex oral/nasal endotracheal tubes because of a manufacturing defect that results in a smaller diameter, which could potentially lead to inadequate ...

The FDA has labeled Smiths Medical's recall of ProPort Implantable Plastic Port as Class I, the most serious kind.

The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as Class I following reports of four patient deaths.

Recalls of food and products, have popped up in the news more recently, with many news reports warning users to check their pantries. This has caused much alarm among consumers who read about them ...

ICU Medical has juggled multiple Smiths recalls and quality issues since acquiring the business in 2022 from London-based conglomerate Smiths Group to expand its lineup of infusion therapy products.