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Medline

MEDLINE INDUSTRIES, INC. · Model DYND17403 · UDI-DI 10080196998401

FFGFON Prescription
10
510(k) clearances
557
Adverse events
1
Recalls
37
Facilities

Description

METER,URINE,DRAIN BAG,400 ML,LF

Recalls

DateFirmReason
2023-12-04Cardinal Health 200, LLCConvenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.

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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.