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Medline

MEDLINE INDUSTRIES, INC. · Model DYND30212 · UDI-DI 10080196997442

OIEFMH
0
510(k) clearances
10
Adverse events
2
Recalls
47
Facilities

Description

KIT,MIDSTREAM,FUNNEL,BZK,30Z PNEUM CUP

Recalls

DateFirmReason
2026-07-09Medical Action Industries, Inc. 306An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027.
2014-04-17Gen-Probe IncIncorrect labeling was used on each pouch of the affected lots of APTIMA Urine Specimen Collection Kits. The outer box of the kits are identified correctly as "APTIMA Urine Collect

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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.