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ADVIA Centaur® AFP

Siemens Healthcare Diagnostics Inc. · Model 10998577 · UDI-DI 00630414022963

LOK
0
510(k) clearances
160
Adverse events
1
Recalls
10
Facilities

Description

Alpha-Fetoprotein (AFP) Assay Kit (1-pack) 100T

Recalls

DateFirmReason
2003-06-12Abbott Laboratories HPD/ADDAFP results obtained when using the 1:101 automated dilution protocol showed an overestimation of AFP of up to 30.5%

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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.