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V. Mueller

STERIS CORPORATION · Model RH550-271 · UDI-DI 10885403109447

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

Description

V. Mueller KENNEDY-LUSK BIOPSY AND GRASPING FORCEPS withSUCTION CHANNEL, STRAIGHT WORKING LENGTH 4 inches 10 CM

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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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.