Klein Foods Cookie Dough Fudge Recall: Potential Food-Grade Rubber Pieces
Klein Foods recalls 1/2 pound cookie dough fudge boxes from August 14, 2019, due to possible food-grade rubber pieces. Consumers should check lot code 918014C.
Use caution until it’s fixed
Product is being recalled due to the potential presence of food-grade rubber pieces.
Contact the company
What happened, in plain English
Klein Foods is recalling 1/2-pound cookie dough fudge boxes produced on August 14, 2019, because they may contain food-grade rubber pieces. This could pose a choking hazard for young children. Read more at govinfonow.com/recall/16375-klein-foods-cookie-dough-fudge-recall-potential-food-grade-rubber.
Source Summary by GovInfoNow · govinfonow.com/recall/16375-klein-foods-cookie-dough-fudge-recall-potential-food-grade-rubber · Updated October 5, 2026 · FDA enforcement record: FDA #F-0331-2020
Cite this page
“Klein Foods Cookie Dough Fudge Recall: Potential Food-Grade Rubber Pieces.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16375-klein-foods-cookie-dough-fudge-recall-potential-food-grade-rubber. Based on FDA recall #F-0331-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0331-2020%22&limit=1).
Why it’s dangerous
The fudge may contain small food-grade rubber pieces that could be a choking hazard for young children. These pieces are not designed to be eaten and could cause injury if swallowed.
Who’s affected
Parents and caregivers of young children who have purchased the recalled fudge boxes are most at risk due to the potential choking hazard.
How to tell if you have this one
Check for the lot code 918014C on the box, which was produced on August 14, 2019. The product is sold in 1/2-pound boxes.
- Brand
Klein Foods- Category
Food
What to do — step by step
Check Product
Look for the lot code 918014C on the box, which was produced on August 14, 2019.
Where it went and when
Where it was distributed
Distributed in Minnesota.
FDA distribution: “The firm distributed the product to two customers located in MN, as well as sold product in their onsite retail store.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- 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-0331-2020 (November 4, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0331-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.