Class I recall

FDA
MedTech

FDA flags J&J Medtech detachable coils most serious recall

The FDA has flagged J&J Medtech’s recall of Cerepak detachable coils as Class I in the wake of one death and four serious injuries.
Joseph Keenan Feb 9, 2026 11:00am
FDA

GAO finds FDA staffing shortfalls delaying device recall work

Dec 12, 2025 3:10pm
Dexcom G6 receiver

Dexcom hit by FDA Class I recall for its CGM system app

Nov 5, 2025 8:45am
X-ray of lungs

Olympus updates corrective action related to 2023 lung scope recall

Nov 4, 2025 8:00am
MRI scan

Siemens Healthineers’ MRIs see FDA recall over ice blockages

Oct 1, 2025 10:30am
heart over ekg

FDA updates recall for Boston Scientific implanted defib leads

Sep 15, 2025 11:55am