Item 404700, UPC 13454 38075, Premium Street Taco Kit With Trays, 2/4.9875 lbs.
Reser's Fine Foods, Inc. recalled this product and the FDA reported the enforcement action on 6 November 2024 as Class II. The recall was initiated by the firm. Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes

The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Item 404700, UPC 13454 38075, Premium Street Taco Kit With Trays, 2/4.9875 lbs. Distributed by Fresh Creative Foods Vista, CA.
- UPC
- 1345438075
- Reason for recall
- Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
- Recalling firm
- Reser's Fine Foods, Inc.
- Firm location
- Beaverton, Oregon, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0087-2025
- Quantity
- 4100 cases
- Distribution
- The firm distributed meal kits directly in AL, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, ME, MD, MA, MI, MO, NE, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WY.
- Initiated
- 10 October 2024
- Reported by FDA
- 6 November 2024
- Terminated
- 12 February 2025
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Use By Dates: 9/2/2024 9/5/2024 9/9/2024 9/13/2024 9/16/2024 9/20/2024 9/23/2024 9/27/2024 10/1/2024 10/4/2024 10/8/2024 10/10/2024 10/11/2024 10/15/2024 10/17/2024 10/25/2024 10/27/2024 10/29/2024 11/1/2024 11/4/2024 11/7/2024 Batch Numbers: B1725633 B1725635 B1725650 B1725652 B1725661 B1725698 B1725706 B1725721 B1731691 B1731693 B1731734 B1731762 B1731791 B1731796 B1731813 B1736530 B1739897 B1739954 B1739973 B1739978 B1739991 B1740625 B1740626 B1740645 B1740745 B1740747 B1742832 B1743972 B1743974 B1743978 B1746240 B1746244 B1746247 B1746253 B1746255 B1755996 B1755998 B1756000 B1756017 B1756032 B1756877 B1756879 B1756889 B1756958 B1757012 B1757022 B1757054 B1762668 B1762678 B1762695 B1763812 B1763813 B1763819 B1763842 B1763845 B1763872 B1764506 B1764507 B1764508 B1764518 B1764519 B1770247 B1770284 B1770287 B1770304 B1770310 B1770312 B1771390 B1771391 B1771403 B1779370 B1779468 B1779470 B1779484 B1785266 B1785271 B1785272 B1785274 B1785281 B1785284 B1785312 B1785331 B1785333 B1785345 B1785361 B1786891 B1786942 B1786945 B1788135 B1788140 B1791550 B1791569 B1791572 B1791584 B1791618 B1792771 B1792777 B1792786 B1792789
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 18 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 18 separate recalls, which almost every published figure does, overstates it by a factor of 18. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 18 of them.
- The recall ran for 4 months, from 10 October 2024 to termination on 12 February 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 29 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Missouri, Nebraska, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wyoming. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Listeria monocytogenes
Listeria monocytogenes is a bacterium that grows at refrigeration temperature, which is why it dominates recalls of ready-to-eat foods that are never cooked again before they are eaten.
A preventive controls plan covers Listeria contamination under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(3)
- Sanitation controls: the controls on cleaning food-contact surfaces and on preventing cross-contact and cross-contamination from insanitary objects, people and equipment.
- 21 CFR 117.165(a)(3)
- Environmental monitoring: testing the processing environment for an environmental pathogen, required when a ready-to-eat food is exposed to the environment before packaging.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Other records from Reser's Fine Foods, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 283 other records name this firm.
All 284 records for Reser's Fine Foods, Inc.
All 2024 recalls · All FDA food recall data
21 CFR 117.135(c)(3) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.