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Anti-Gliadin (GAF-3X) ELISA (IgG)

EUROIMMUN Medizinische Labordiagnostika AG · Model EV 3011-9601 G · UDI-DI 04049016035954

MST
1
510(k) clearances
0
Adverse events
3
Recalls
20
Facilities

Recalls

DateFirmReason
2023-05-01Phadia US IncHigher reported results when running EliA GliadinDP IgG Well on the instruments Phadia 2500EE compared to running EliA GliadinDP IgG Well on Phadia 250 instrument
2023-05-01Phadia US IncHigher reported results when running EliA GliadinDP IgG Well on the instruments Phadia 2500EE compared to running EliA GliadinDP IgG Well on Phadia 250 instrument
2008-03-21Diamedix CorporationStandards and controls in the Is-anti-Gliadin IgG Test Kits are exhibiting low activity. A drop in the O.D.s the Positive Control could potentially recover low out of range (which

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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.