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Medline
MEDLINE INDUSTRIES, INC. · Model NON1569473FC · UDI-DI 10080196408665
5
510(k) clearances
1
Adverse events
1
Recalls
71
Facilities
Description
DBD-COT,FINGER,MEDIUM,CUSTOM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2016-03-31 | American Surgical Company | Product packaging defective compromising sterility |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.