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RZ Medizintechnik GmbH

RZ-Medizintechnik GmbH · Model 252-529-120 · UDI-DI 04049197176972

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

Description

Watson-Williams Ethmoidal Forceps Fig. 1 WL 115mm, 4 1/2"

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.