FDA recall record

RMJV, LP dba Fresh Creative Foods Fresh Creative Foods RED SAUCE CHICKEN ENCHILADA KIT ON recall — FDA F-0895-2022

During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.

Class IIclassification
F-0895-2022official record ID
Mar 23, 2022report date

Recall record at a glance

Official recordF-0895-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRMJV, LP dba Fresh Creative Foods
Report dateMar 23, 2022
Recall initiation dateMar 7, 2022
Quantity171 cases
LocationVista, CA, United States

Official product description

Fresh Creative Foods RED SAUCE CHICKEN ENCHILADA KIT ON PREMISE NO TRAYS 2/6.75 LB UPC: 10013454381929 Item # 404979 Perishable/Keep refrigerated Kit components: 2/32 oz. bags of seasoned chicken w/rib meat, 8/8 pz. bags of Cryo Traditional Red Enchilada Sauce, 8 bags of golden blend 6" tortillas, 4/8 oz. bags of cheddar * Monterey Jack Cheese blend fancy shredded, 1 sheet label #5154 Red Sauce Chicken enchilada Distributed by Fresh Creative Foods, Vista, CA Information: A prepackaged bag of RTE is chicken is purchased from a USDA establishment. The packaged chicken is not opened or further processed when we make the kits. The kit consists of unopened packages of components such as the chicken, sauce, tortillas and cheese and the customer opens the components, assembles the ingredients and sells it. Based on the chicken staying in the enclosed bag, fully labeled for USDA compliance including a mark of inspection, the kit is excluded from USDA oversite.

Why the product was recalled

During manufacturing pieces of hard clear plastic was found. Upon investigation the source was identified as ice purchased from supplier.

Distribution information

AR, AZ, CA, CO, FL, GA, IL, IN, KY, MN, MO, NC, NV, OH, OK, OR, SC, TN, TX, WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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