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AESCULAP

AESCULAP, INC. · Model MA245R · UDI-DI 04046964585746

KAE Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities

Description

HARTMANN-HERZFELD Ear Forceps, 5 1/8", (130 mm), (71 mm), (1,50 mm), 0,6 x 1 mm cup

Recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.