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STERIS CORPORATION · Model enspire 3000 Maxflow Connector · UDI-DI 00724995229016

FEB

510(k) clearances

5,046

Adverse events (22 deaths)

Recalls

Facilities

Description

enspire 3000 MaxFlow Connector, ENLCS633

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	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.
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.

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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.