FDA recall record

Reser's Fine Foods ***Chicken Street Taco Kit with Trays, item # 13454.38080 recall — FDA F-0655-2021

Undeclared egg. The cup of Chipotle Crema in the Chicken Street Taco kits contains undeclared egg.

Class Iclassification
F-0655-2021official record ID
Jun 9, 2021report date

Recall record at a glance

Official recordF-0655-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmReser's Fine Foods, Inc.
Report dateJun 9, 2021
Recall initiation dateMay 21, 2021
QuantityTotal 35,571 cases (item #38080 = 6,979 cases; item # 30435 = 1,366 cases; item # 38082 = 27,226 cases).
LocationBeaverton, OR, United States

Official product description

***Chicken Street Taco Kit with Trays, item # 13454.38080, Refrigerated product, 2/4.985 lbs. kits in each case. Distributed by Reser's Fine Foods, Topeka, KS. ***Homechef Chicken Street Taco Kit with Trays, item # 40134.30435, Refrigerated product, 2/4.985 lbs. kits in each case. Distributed by Reser's Fine Foods, Topeka, KS. Kit Components (with trays): 2/32 oz. bags of Grilled Chicken. 2 bags of White Corn Blend Tortillas. 2 sleeves of 4/2oz. cups of Chipotle Crema. 2 sleeves of 4/2oz. cups of Salsa. 2/8oz. bags of Cheddar & Monterrey Jack Cheese Blend. 1 bag of 8 full trays Combo with Clear Vented Lid. ***Chicken Street Taco Kit without Trays, item # 13454.38082, Refrigerated product, 2/4.985 lbs. kits in each case. Distributed by Reser's Fine Foods, Topeka, KS. Kit Components (without trays): 2/32 oz. bags of Grilled Chicken. 2 bags of White Corn Blend Tortillas. 2 sleeves of 4/2oz. cups of Chipotle Crema. 2 sleeves of 4/2oz. cups of Salsa. 2/8oz. bags of Cheddar & Monterrey Jack Cheese Blend.

Why the product was recalled

Undeclared egg. The cup of Chipotle Crema in the Chicken Street Taco kits contains undeclared egg.

Distribution information

distributed in AL, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, NC, NE, OH, OK, PA, TN, TX, VA, and WI.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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