FDASeptember 19, 2022device

Atellica CH Lithium (Li), Siemens Material Number 11097535. in vitro diagnostic assay

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

The hazard

Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930 Analyzer. In the worst case, there is a potential for erroneously elevated lithium patient results, which may lead to inappropriate dosage adjustment, potentially affecting treatment efficacy.

What to do

FDA enforcement status: Ongoing

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

UPCs

00630414006789

Recall history

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

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Atellica CH Lithium (Li), Siemens Material Number 11097535. in vitro diagnostic assay — Recall Details · AllClear