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Remel, Inc recalls remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use
Recalled February 26, 2025 · FDA recall Z-1200-2025 · Remel
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. · FDA Class II
Units
787 units
Sold at
US Nationwide distribution.
Description
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.
Product
remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use
Manufacturer(s)
Remel, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →