Home › WELCH ALLYN, INC. › Welch Allyn, Inc.
Welch Allyn, Inc.
WELCH ALLYN, INC. · Model 901117 · UDI-DI 00732094239331
FER
Prescription
10
510(k) clearances
86
Adverse events
1
Recalls
46
Facilities
Description
Obturator Assembly, for Model 33020 Fiber Optic/Stricture, Speculum
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-12-12 | Applied Medical Resources Corp | Unintentional shifting of the tip insulation of the firm's electrosurgical probes. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.