Class II
Medical Device Recall: remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use
Remel, Inc · February 13, 2025
Reason for Recall
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.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
787 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1200-2025
Status: ongoing
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