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Argyle
Cardinal Health, Inc. · Model 8888257360 · UDI-DI 20884527000118
9
510(k) clearances
33
Adverse events
1
Recalls
64
Facilities
Description
Mucus Trap with Vacuum Breaker,10 Fr/Ch (3.33 mm), Catheter
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-11-04 | Medline Industries Inc | There is a potential that the specified mucus specimen traps are not sterile. Use of the affected products may result in the contamination of patient specimens. |
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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.