FDAFebruary 13, 2018device

FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System

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

The hazard

Module may freeze without generating user warning. There is a potential risk in delay of sample processing, leading to delayed delivery of test results to patients.

What to do

FDA enforcement status: Terminated

Brands named

inpeco

Recall history

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

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