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VIALMIX®RFID

LANTHEUS MEDICAL IMAGING, INC. · Model VMIX2 · UDI-DI 00866709000402

EFD
10
510(k) clearances
6
Adverse events
1
Recalls
32
Facilities

Description

Class I medical device, Amalgamator, Dental, AC-powered. Used to activate vials of DEFINITY® RT, and DEFINITY®, Vial for (Perflutren Lipid Microsphere) Injectable Suspension prior to use.

Recalls

DateFirmReason
2026-07-20SDI LimitedPotential for electrical discharge from unit when unplugged.

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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.