Caplugs/Evergreen
CAPlugs · Model 127-0080-R10 · UDI-DI 00810044200560
10
510(k) clearances
354
Adverse events (2 deaths)
1
Recalls
18
Facilities
Description
8.5 mL Serum Sample Cups
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-08-24 | Hamilton Co | The product valve has a high probability of deforming and may result in leakage during use. |
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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.