The FDA issued a notice identifying a high-risk device issue associated with a Medtronic recall of Bravo CF capsule delivery ...

The FDA is amplifying a recall from Medtronic for its acid reflux testing system, after the company said it received 33 ...

8/12: CBS News 24/7 Episode 2 43:20. In 2016, medical device giant Abbott issued a recall for its MitraClip cardiac device — "a Class I recall, the most serious type," the FDA said. "Use of this ...

Relating to certain of Medtronic’s Newport ventilator range, users have been advised to remove the affected units from ...

The FDA has designated Cook Medical's recall of its Beacon Tip 5.0 Fr angiographic catheter as Class I, the most serious ...

Coating for the guidewires could come off and get left in patients, which could result in extended or additional procedures.

FDA highlights risks from recalled Medtronic devices tied to esophageal injuries and faulty cannulas, with serious health ...

With medical devices, recalls are not always what they seem. In some recalls, including some of the most serious, the FDA and the manufacturers let doctors and hospitals continue to use the devices.

In 2016, medical device giant Abbott issued a recall for its MitraClip cardiac device — “a Class I recall, the most serious type,” the FDA said. “Use of this device may cause serious ...

In 2016, medical device giant Abbott issued a recall for its MitraClip cardiac device—“a Class I recall, the most serious type,” the FDA said. “Use of this device may cause serious ...

In 2016, medical device giant Abbott issued a recall for its MitraClip cardiac device — “a Class I recall, the most serious type,” the FDA said. “Use of this device may cause serious injuries or death ...