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Alinity

Abbott GmbH · Model 09P5920 · UDI-DI 00380740150686

DAD Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Alinity c Haptoglobin Reagent Kit 180 Tests

Recalls

Date	Firm	Reason
2018-05-16	Abbott Laboratories, Inc	An 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.