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ARCHITECT

ABBOTT IRELAND · Model 04U4530 · UDI-DI 00380740155490

CJW Prescription
10
510(k) clearances
17
Adverse events
1
Recalls
24
Facilities

Description

Albumin BCP2 2200 Tests

Recalls

DateFirmReason
2019-03-18Roche Diagnostics CorporationThe reagent lot is exhibiting calibration failures, QC imprecision, and elevated QC recovery due to elevated pH level causing higher absorbance values.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.