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Welch Allyn, Inc.

WELCH ALLYN, INC. · Model 901025 · UDI-DI 00732094074192

HJN Prescription
3
510(k) clearances
24
Adverse events
1
Recalls
28
Facilities

Description

Welch Allyn 3.5 V Finoff Transilluminator

Recalls

DateFirmReason
2005-04-28Venoscope LLCExcessive heating due to incorrect wire assembly process.

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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.