FDA campaign H-0686-2026
Class IHazard
product tested positive for Listeria Monocytogenes.
Distribution
5 direct account consignees located in CA, FL and MD.
REKALLD area-alert coverage: nationwide (our reading of the distribution above)
The text above is quoted verbatim from the FDA record. Confirm the affected units and the remedy with the manufacturer or FDA. Recall data may be incomplete, delayed, or superseded.