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DOMICO MED-DEVICE, LLC · Model 20162 · UDI-DI 00810050242202
10
510(k) clearances
44
Adverse events
1
Recalls
49
Facilities
Description
SYSTEM, UROLOGY BAG SUPPORT
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-09 | C.R. Bard, Inc. | Misbranded: Product labeled, Not made with natural rubber latex, may in fact contain natural rubber latex. |
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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.