The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.

Olympus has recalled endoscope guide sheath kits after receiving 26 reports of serious injuries linked to the devices. The Food and Drug Administration, which published a Class I recall notice ...

While the city council has agreed to move ahead with Porrit's plan, for now, should the recall pass for the three members of the council, Richard at least has sworn to slow things down ...

Medical device recall events in 2024 reached their highest level since 2020 and more than 10% of them involved the most serious type of recall. There were 1,048 medical device recalls in 2024 ...

The devices are being recalled due to an increased risk for permanently entering Safety Mode. HealthDay News — Boston Scientific has issued a recall of Accolade pacemaker devices, according to a ...

TUESDAY, Feb. 25, 2025 (HealthDay News) — Boston Scientific has issued a recall of Accolade pacemaker devices, according to a safety communication from the U.S. Food and Drug Administration. The ...

TUESDAY, Feb. 25, 2025 (HealthDay News) -- Boston Scientific has issued a recall of Accolade pacemaker devices, according to a safety communication from the U.S. Food and Drug Administration.

Boston Scientific has issued a recall of Accolade pacemaker devices, according to a safety communication from the U.S. Food and Drug Administration. The Accolade devices under recall include the ...