FDA Device Intelligence
HomeMCKESSON MEDICAL-SURGICAL INC. › McKesson

McKesson

MCKESSON MEDICAL-SURGICAL INC. · Model 63-6341 · UDI-DI 00612479217195

OHY
0
510(k) clearances
38
Adverse events
1
Recalls
95
Facilities

Description

Pill Cutter

Recalls

DateFirmReason
2022-05-11MEDLINE INDUSTRIES, LP - NorthfieldProduct lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.

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.