FDAJune 22, 2022device

Revogene, Catalog no. 610210. IVD test instrument

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

The hazard

When a run is aborted, the cooling period protection does not occur and the user is able to open the lid prior to the completion of the cooling period, exposing the user to heated instrument components. Incidental contact with heated instrument components may result in an injury such as minor burns.

What to do

FDA enforcement status: Ongoing

Brands named

meridian biosciencemeridian

UPCs

00840733102318

Recall history

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

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Revogene, Catalog no. 610210. IVD test instrument — Recall Details · AllClear