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WESTMED, INC. · Model 6159 · UDI-DI 00709078001017
MOD
Prescription
10
510(k) clearances
19
Adverse events (1 deaths)
1
Recalls
8
Facilities
Description
Hepa Filter, W/CO2 Port
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-06-08 | Medical Device Group Inc. | Device separation presenting a choking hazard. |
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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.