FDA Food recall ·
Item 401311 recall
This is an FDA Class I recall — the most serious type.
- Recall number
- F-0088-2025
- Date
- (initiated October 10, 2024)
- Company / brand
- Reser's Fine Foods, Inc.
15570 SW Jenkins Rd, Beaverton, OR, United States - Category
- Food › Class I
- Classification
- Class I
- Status
- Terminated
- Units affected
- 21,098 cases
- Hazard tags
- Listeria Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Item 401311, UPC 13454 35855, Caesar Salad Kit 2/6 lbs. Distributed by Fresh Creative Foods Vista, CA.
Why was it recalled?
Meal kits contain cooked chicken which was recalled due to contamination with Listeria monocytogenes
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Batch numbers: B1739939 B1743145 B1744875 B1744878 B1750691 B1750774 B1750788 B1751973 B1751977 B1754609 B1758347 B1759723 B1759734 B1761252 B1763990 B1764925 B1767173 B1772003 B1772023 B1772285 B1775211 B1778486 B1780217 B1782248 B1783619 B1784054 B1784405 B1787510 B1790164 B1791661 B1793587 B1795392 B1796231
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.
States: Alabama Arizona California Colorado Florida Georgia Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Missouri North Carolina Nebraska New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wyoming
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (food), recall F-0088-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.