FDAMay 12, 2020device

MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended for use on the LIAISON MDX instrument for the qualitative detection of varicella-zoster virus (VZV) DNA present in cutaneous and mucocutaneous lesion swabs from patients with signs and symptoms of VZV infection.

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

The hazard

Due to a software malfunction in the Multi Assay Suite, there is the probability of increased occurrence of false negative results.

What to do

FDA enforcement status: Terminated

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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MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended for use on the LIAISON MDX instrument for the qualitative detection of varicella-zoster virus (VZV) DNA present in cutaneous and mucocutaneous lesion swabs from patients with signs and symptoms of VZV infection. — Recall Details · AllClear