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Atellica CH HAPT2

Siemens Healthcare Diagnostics Inc. · Model 11537232 · UDI-DI 00630414610986

DAD
10
510(k) clearances
1
Adverse events
1
Recalls
31
Facilities

Description

Haptoglobin (HAPT2) Atellica CH

Recalls

DateFirmReason
2018-05-16Abbott Laboratories, IncAn update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.

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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.