FDANovember 4, 2024device

Atellica CI Analyzer. Catalog Numbers: 10947347.

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

The hazard

Potential that the IMT Diluent volume remaining (% remaining) does not decrease as expected on the Atellica CI Analyzer, potentially leading to the IMT Diluent being empty while still displaying that volume is remaining. In this case Sodium (Na), Potassium (K) and Chloride (Cl) test results may be falsely elevated. Quality Control materials demonstrate the same behavior.

What to do

FDA enforcement status: Ongoing

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

UPCs

630414229560

Recall history

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

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