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Anti-M2-3E ELISA (IgG)

EUROIMMUN Medizinische Labordiagnostika AG · Model EA 1622-9601 G · UDI-DI 04049016027157

DBM
1
510(k) clearances
1
Adverse events
2
Recalls
17
Facilities

Recalls

DateFirmReason
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.
2004-04-12Diasorin Inc.The data reduction program written for a specific automated microtiter plate instrument (Bio-Tek ELx800 reader) was found to be faulty. This program is used to calculate the cut o

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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.