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ANA IFA: HEp-20-10

EUROIMMUN Medizinische Labordiagnostika AG · Model FA 1522-1005 · UDI-DI 04049016045342

DHN
1
510(k) clearances
1
Adverse events
7
Recalls
19
Facilities

Recalls

DateFirmReason
2011-09-26Inova Diagnostics IncorporatedThe NOVA Lite ANA KSL kit label has the wrong fill volume for the IFA System Negative Control (P/N 508186) with 1mL. The component in the kit is correctly labeled and filled with
2010-06-30Bio-Rad LaboratoriesKALLESTAD Mouse Stomach/Kidney (MSK) test kits contained Crithidia slides instead of the MSK slides.
2008-12-04Immuno Concepts IncSamples can occasionally run out of the wells and cross contaminate adjacent wells.
2008-07-29Bio-Rad LaboratoriesThe Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit.
2004-09-24Diasorin Inc.A problem with software for the PolyTiter Immunofluorescent Titration System in that no flags or warnings appear when PolyTiter Calibrator Values are re-entered or changed (includi
2004-06-30Diasorin Inc.The program for a specific immunofluorescent titration system (Polymedco PolyTiter immunofluorescent Titration System) was found faulty in that the calibrator 2 value was incorrect
2003-07-21Perkinelmer Life Sciences, Inc.Product's outer carton label was labeled with an extended expiration date

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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.