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ARCHITECT

ABBOTT IRELAND · Model 04T1330 · UDI-DI 00380740158361

CDO Prescription
10
510(k) clearances
0
Adverse events
1
Recalls
6
Facilities

Description

Uric Acid2 2000 Tests

Recalls

DateFirmReason
2004-03-18Abbott Laboratories Diagnostic DivUnacceptable upward drift of results in control runs within 24 hour period.

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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.