FDAMarch 29, 2022device

VITEK 2 Systems and VITEK 2 with MYLA.

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

The hazard

Software issue where results sent to the LIS via HL7 format for antibiotic screen tests and synergy tests do not include the user-corrected or AES-corrected interpretation. This can potentially lead to incorrect final screen/synergy test results at the LIS.

What to do

FDA enforcement status: Ongoing

Brands named

biomerieux

Recall history

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

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VITEK 2 Systems and VITEK 2 with MYLA. — Recall Details · AllClear