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Medline
MEDLINE INDUSTRIES, INC. · Model DYND10806 · UDI-DI 10080196028856
EYZ
Prescription
10
510(k) clearances
44
Adverse events
1
Recalls
50
Facilities
Description
KIT,SPECI-CATH,MINI,FEMALE,8FR,PVP,GLVS
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.