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Overbed Table H Base, Silver Vein, Walnut
Dynarex Corporation · Model 10450-WN · UDI-DI 00840117340213
10
510(k) clearances
18
Adverse events (2 deaths)
1
Recalls
103
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-05-30 | Chattanooga Corp. | Product contains an improper bracket for the transducer. |
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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.