FDAJuly 12, 2021device

Alinity s System REF 06P16-01. An automated immunoassay analyzer for In Vitro diagnostic use in blood donor screening, plasma and plasmapheresis screening, and organ donor centers, hospitals, and reference laboratories.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

A design defect (hardware and software) allows liquid waste pressure to build up and potentially spray users/operators.

What to do

FDA enforcement status: Ongoing

Brands named

abbott laboratoriesabbott

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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