FDAMarch 20, 2024device

Alinity m System, Part Number: 08N53-002

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

The hazard

The Alinity m System camera detects whether tubes are "capped." If the camera detects a cap and the retention bar is not present on the sample rack, the system will generate the message 'Error - 6013: Has cap, no retention bar." Abbott has identified an issue concerning the use of certain third-party Universal Transport Medium (UTM) tubes on the Alinity m System. This issue has been observed with Copan UTM-RT 3 mL Without Beads Transport & Preservation Medium for Viral Molecular Diagnostics Testing, Part Number (PN) 3C047N. However, it is possible that other third party manufactured tubes could experience the same issue.

What to do

FDA enforcement status: Ongoing

Brands named

abbott molecularabbott

UPCs

00884999048034

Recall history

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

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