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McKesson

MCKESSON MEDICAL-SURGICAL INC. · Model 122-LBXL · UDI-DI 20612479267910

OMD Prescription
1
510(k) clearances
2,179
Adverse events (2 deaths)
0
Recalls
14
Facilities

Description

LiquiBand® XL Skin Closure System

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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.