Let's Do Lunch Chili Dog Recall: Listeria Risk
Let's Do Lunch recalls Low Fat/Low Sodium Chili Dogs due to potential Listeria monocytogenes contamination. Check lot numbers immediately.
Stop using this now
Potential Listeria monocytogenes contamination.
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What happened, in plain English
Let's Do Lunch, Inc. is recalling its Low Fat/Low Sodium Chili Dog (Product ID 952000) because of a potential Listeria monocytogenes contamination. The recall covers 878 cases distributed to California, New Mexico, Ohio, Virginia, Arizona, Michigan, Texas, North Carolina, and Pennsylvania. No foreign distribution was involved. Read more at govinfonow.com/recall/23738-let-s-do-lunch-chili-dog-recall-listeria-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/23738-let-s-do-lunch-chili-dog-recall-listeria-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-2025-2016
Cite this page
“Let's Do Lunch Chili Dog Recall: Listeria Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/23738-let-s-do-lunch-chili-dog-recall-listeria-risk. Based on FDA recall #F-2025-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2025-2016%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacterium that can cause serious and sometimes fatal infections in young children, frail or elderly people, and persons without strong immune systems. Healthy individuals may suffer only short-term symptoms like fever, muscle aches, and gastrointestinal issues such as nausea or diarrhea.
Who’s affected
Consumers in the U.S. who purchased the recalled Low Fat/Low Sodium Chili Dog from retailers in California, New Mexico, Ohio, Virginia, Arizona, Michigan, Texas, North Carolina, or Pennsylvania are likely affected.
How to tell if you have this one
Check if you have the Chili Dog, Low Fat/Low Sodium product with Product ID 952000. Verify the lot numbers on the packaging: 051816D, 052716B, or 052716D.
- Brand
Let's Do Lunch- Category
Food
All 9 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
U.S. distribution to the following; CA, NM, OH, VA, AZ, MI, TX, NC, PA. No foreign distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-2025-2016 | Chili Dog, Low Fat/Low Sodium Product ID 952000; Lot #051816D, 052716B, 052716D | 878 cases |
| F-2026-2016 | Cheeseburger Sliders Product ID C47220, 470220; Lot #051816C, 051916C, 052016C, 052016D, 052316C, 052516D, 052616C | 2,085 cases |
| F-2027-2016 | All American Cheeseburger Product ID 470007; Lot #051916B, 060916D | 207 cases |
| F-2028-2016 | Beef Sausage & Cheese Mini Bagel Sandwich Product ID C80916; Lot #052016C | 32 cases |
| F-2029-2016 | BBQ Rib Sandwich Product ID C46007, 460007; Lot #052416C, 052516B | 687 cases |
| F-2030-2016 | Chicken Patty Sandwich on a Whole Grain Bun Product ID 400003; Lot #052516D | 7 cases |
| F-2031-2016 | Beef Sausage Breakfast Sandwich Product ID C99018; Lot #052416B | 167 cases |
| F-2032-2016 | Chicken Double Dogs on Whole Grain Bun Product ID 809021; Lot #060316D | 253 cases |
| F-2033-2016 | All American Burger Product ID 470007, C47007; Lot #052016D, 052516C, 060916C, 061016C | 590 cases |
What to do — step by step
Stop consuming the product
Do not eat the recalled Chili Dog due to the potential Listeria contamination risk.
Check lot numbers
Verify if your product matches Product ID 952000 and has one of the affected lot numbers: 051816D, 052716B, or 052716D.
Discard or return item
The recall record does not specify the exact remedy steps for consumers, so please contact the manufacturer or retailer for instructions on disposal or refund.
Where it went and when
Where it was distributed
Distributed in 9 states.
FDA distribution: “U.S. distribution to the following; CA, NM, OH, VA, AZ, MI, TX, NC, PA. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Michigan, New Mexico, North Carolina, Ohio, Pennsylvania, Texas, Virginia.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-2025-2016 (July 25, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2025-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.