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Class I recall
MedTech
FDA amplifies neurosurgery kit recall at Medline, Integra
Some 170,000 perforators have been recalled by Integra due to a manufacturing defect that may cause the hardware to break apart during a craniotomy.
Conor Hale
Jul 22, 2025 12:30pm
Dexcom replaces hand-held CGM receivers after missed audio alerts
Jun 17, 2025 10:40am
Smiths Medical recalls infusion pumps over 3 safety risks
Jun 5, 2025 9:46am
Bausch + Lomb identifies cause of intraocular lens recall
May 6, 2025 11:30am
FDA elevates recall as Philips pulls implant from the market
Mar 4, 2025 2:35pm
FDA updates Boston Scientific's serious pacemaker recall
Feb 25, 2025 12:00pm
