Class II
Medical Device Recall: Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Remel, Inc · July 11, 2025
Reason for Recall
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Distribution
US Nationwide distribution.
States Affected
NATIONWIDE
Quantity Affected
1552 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2223-2025
Status: ongoing
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