FDA Device Intelligence
Home › Device types › FEB

Accessories, Cleaning, For Endoscope

FDA product code FEB · Class 2 · Gastroenterology, Urology

669
Registered devices
5,104
Adverse events
43
Recalls
58
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-09-21Steris CorporationIf the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemis
2026-09-21Steris CorporationIf the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemis
2026-09-21Steris CorporationIf the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemis
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasXXX
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25Olympus Corporation of the AmericasPotential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.