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V. Mueller

STERIS CORPORATION · Model W-0583 · UDI-DI 10885403000997

HAE Prescription
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities

Description

V. Mueller INTERVERTEBRAL DISCECTOMY RONGEUR, FENESTRATED 3 X3 12MM DOWN OVERALL LENGTH 7-1/4 inches 185MM

Recalls

DateFirmReason
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.
2023-10-30Folsom Metal Products, Inc.Units were not intended for commercial distribution and inadvertently distributed.

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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.