FDA Device Intelligence
HomeMCKESSON MEDICAL-SURGICAL INC. › McKesson

McKesson

MCKESSON MEDICAL-SURGICAL INC. · Model 63-4476 · UDI-DI 20612479217960

HOY
10
510(k) clearances
49
Adverse events
1
Recalls
719
Facilities

Description

SHIELD, EYE ALUM W/O CVR LF

Recalls

DateFirmReason
2008-06-05Phillips Safety ProductsRadiation Protective Eyewear does not meet the radiation protection levels stated on the labeling.

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.