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Medline

MEDLINE INDUSTRIES, INC. · Model DYND140214 · UDI-DI 10080196183012

EYZOHR Prescription
10
510(k) clearances
45
Adverse events
1
Recalls
49
Facilities

Description

TRAY,FOLEY,SILVER,2-WAY,14FR,10ML,LF

Recalls

DateFirmReason
2017-03-09C.R. Bard, Inc.Misbranded: Product labeled, Not made with natural rubber latex, may in fact contain natural rubber latex.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.