Home › MEDIVATORS INC. › Scope Buddy

Scope Buddy

MEDIVATORS INC. · Model EFA-US-G · UDI-DI 00677964063640

FEB Prescription

510(k) clearances

5,072

Adverse events (22 deaths)

Recalls

Facilities

Description

Scope Buddy Endoscope Flushing Aid

Recalls

Date	Firm	Reason
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	XXX
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
2026-03-25	Olympus Corporation of the Americas	Potential 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 key Read the docs

Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.