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LIAISON® QuantiFERON® Software

DIASORIN SPA · Model Q0001 · UDI-DI 08056771103572

NCD Prescription
0
510(k) clearances
28
Adverse events
3
Recalls
4
Facilities

Recalls

DateFirmReason
2016-02-02Qiagen Sciences LLCPotential for obtaining a false positive result due to the possibility of endotoxin presence.
2012-09-27Cellestis IncCellestis is recalling QuantiFERON - TB Gold TB Blood Collection Tubes and HA TB Blood Collection Tubes due to potential contamination.
2012-09-27Cellestis IncCellestis is recalling QuantiFERON - TB Gold TB Blood Collection Tubes and HA TB Blood Collection Tubes due to potential contamination.

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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.