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ABBOTT IRELAND · Model 09D9224 · UDI-DI 00380740170141

DER Prescription
10
510(k) clearances
3
Adverse events
2
Recalls
11
Facilities

Description

Apolipoprotein A1 243 Tests

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.
2005-11-10Abbott Laboratories Diagnostic DivThese specific protein assays are not meeting the 57-day on board stability claim

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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.