FDA Device Intelligence
HomeSTERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model LAFOG-FT · UDI-DI 10885403231643

OCT Prescription
10
510(k) clearances
181
Adverse events
2
Recalls
61
Facilities

Description

V. Mueller PREMIUM ANTI-FOG WITH FLIP TOP BOTTLE 20 EACH/BOX

Recalls

DateFirmReason
2022-01-14Sunstar Americas, Inc.Product lacks premarket clearance.
2019-05-30Medline Industries, Inc.The Anti-Fog Solution may not defog properly due to a degradation in the chemical properties.

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
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.