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AESCULAP

AESCULAP, INC. · Model MA413R · UDI-DI 04046964586996

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

Description

WILLIAMS Lacrimal Probe, 5 1/2" (140 mm), double ended, #5/6

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.