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ORTHO

ORTHO-CLINICAL DIAGNOSTICS, INC. · Model 6902412 · UDI-DI 10758750007745

MIU Prescription
6
510(k) clearances
46
Adverse events
1
Recalls
11
Facilities

Description

T. CRUZI ELISA TEST SYSTEM 192T WW

Recalls

DateFirmReason
2017-11-10Wiener LaboratoriesInternal program testing shows that product may not reach the indicated 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.