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McKesson

MCKESSON MEDICAL-SURGICAL INC. · Model 140-MED · UDI-DI 10612479220574

MLY Prescription

510(k) clearances

Adverse events (2 deaths)

Recalls

Facilities

Description

Topical Anesthetic Spray Medium Stream

Recalls

Date	Firm	Reason
2008-09-03	Gebauer Company	Some 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
2007-04-17	Gebauer Company	Mold contamination
2007-04-17	Gebauer Company	Mold contamination
2007-04-17	Gebauer Company	Mold contamination
2007-04-17	Gebauer Company	Mold contamination
2007-04-17	Gebauer Company	Mold contamination
2007-04-17	Gebauer Company	Mold contamination

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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.