FDANovember 19, 2021device

Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455

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

The hazard

A subset of affected discs are at risk of leakage when it is used more than one time with Simplexa COVID-19 Direct and/or Simplexa Flu A/B & RSV Direct Gen II. Leakage from a well that had a positive sample may cause further cross-contamination in areas of the lab if not properly cleaned.

What to do

FDA enforcement status: Ongoing

Brands named

diasorin moleculardiasorin

Recall history

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

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