FDAJune 28, 2019device

Alinity c Lithium Reagent Kit- intended for the quantitation of lithium in serum or plasma using respectively the ARCHITECT c Systems and the Alinity c analyzer List Number: 08P5320

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

The hazard

Added an additional SmartWash parameter for the Lithium and Alinity c Lithium Reagent Kit, catalogue number 8L25-30 and 08P5320 to prevent the potential for carryover from the ARCHITECT Lactate Dehydrogenase (LDH) reagent (LN 2P56) may result infalsely elevated lithium patient results

What to do

FDA enforcement status: Terminated

Brands named

sentinel ch spasentinelsentinel ch

UPCs

003807401362770038074013627

Recall history

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

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