FDAFebruary 13, 2025device

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

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

The hazard

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

What to do

FDA enforcement status: Ongoing

Brands named

remel

UPCs

848838003691

Recall history

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

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