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DualCap®

Merit Medical Systems, Inc. · Model 10884450309367 · UDI-DI 10884450309367

QBP
10
510(k) clearances
24
Adverse events (1 deaths)
2
Recalls
30
Facilities

Recalls

DateFirmReason
2025-06-16MEDLINE INDUSTRIES, LP - NorthfieldSwabFlush syringes are affected by the ICU Medical recall of their SwabCap Disinfecting Cap due to a manufacturing issue which affects the seal between the foil lid and plastic con
2025-06-03ICU Medical, Inc.Due to a manufacturing issue, disinfecting cap for needle-free connectors may have an incomplete seal between the foil lid and plastic container, which may result in isopropyl alco

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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.