FDAOctober 12, 2022device

Alinity m System, REF 08N53-002, For In Vitro Diagnostic Use

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

The hazard

Abbott has identified potential performance issues for the Alinity m System software version 1.6.5: 1) In a unique scenario, the waste chute flapper was found to not open when the Systems Solution drawer was closed and locked. It was found that the software will cause the flapper door to stay in the closed position when the drawer is closed and locked if the flapper had previously been moved out of position. 2) Sample preparation drawer #1 barcode information is used instead of sample prep drawer #2 when the scanned data is not sent to the System Control Center before the next bottle barcode in sample prep drawer#2 is scanned. 3) Under a specific condition, while the system is processing tests and a new test request is made, when the level of the bulk solution is too low to process a test, the software would error stop the system and try to complete all in-process tests. An internal counter is reset which can cause reaction vessels (RVs) already present in an Amplification Detect

What to do

FDA enforcement status: Ongoing

Brands named

abbott molecularabbott

Recall history

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

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