Class II
Medical Device Recall: Strep Selective II Agar, Product Number R01859
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
371 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2224-2025
Status: ongoing
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