Home › MEDLINE INDUSTRIES, INC. › MEDLINE
MEDLINE
MEDLINE INDUSTRIES, INC. · Model DYND44110 · UDI-DI 10080196997404
BYZ
Prescription
9
510(k) clearances
26
Adverse events
1
Recalls
63
Facilities
Description
TRAP,MUCUS, 10FR, DELEE, W/VALVE
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. |
Query this across every FDA database — by API.
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.