FDA Device Intelligence
HomeMCKESSON MEDICAL-SURGICAL INC. › McKesson

McKesson

MCKESSON MEDICAL-SURGICAL INC. · Model 140-MST · UDI-DI 10612479220598

MLY Prescription
10
510(k) clearances
24
Adverse events (2 deaths)
7
Recalls
19
Facilities

Description

Topical Anesthetic Spray Mist

Recalls

DateFirmReason
2008-09-03Gebauer CompanySome units of Fluro-Ethyl containing the defective valve which could malfunction and spray refrigerant out from the side of the valve in addition to or instead of spraying in the n
2007-04-17Gebauer CompanyMold contamination
2007-04-17Gebauer CompanyMold contamination
2007-04-17Gebauer CompanyMold contamination
2007-04-17Gebauer CompanyMold contamination
2007-04-17Gebauer CompanyMold contamination
2007-04-17Gebauer CompanyMold contamination

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.