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Welch Allyn, Inc.
WELCH ALLYN, INC. · Model 901006 · UDI-DI 00732094336177
BZG
Prescription
1
510(k) clearances
31
Adverse events
1
Recalls
94
Facilities
Description
CPWS AM12 RESTING ACCESSORIES IN DISPLAY
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-10-11 | Baxter Healthcare Corporation | There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System |
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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.