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AESCULAP

AESCULAP, INC. · Model MA407R · UDI-DI 04046964586941

HNL Prescription
10
510(k) clearances
40
Adverse events
1
Recalls
155
Facilities

Description

BOWMAN Lacrimal Probe, 6" (150 mm), double ended, #0000/000

Recalls

DateFirmReason
2015-02-26Quest Medical, Inc.Expiration date incorrectly printed in Manufacturing Date field on both pouch and carton labels

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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.