Lutosa Plain Mashed Potatoes Recall: Foreign Plastic/Rubber Pieces Risk
Lutosa Foodservice Quality Plain Mashed potatoes from Belgium (2.5kg) with specific lot numbers may contain plastic and rubber pieces. Consumers should check lot numbers and contact Lutosa for details.
Lower-risk recall
Potential foreign object; plastic and rubber pieces.
Contact the company
What happened, in plain English
Lutosa Foodservice Quality Plain Mashed potatoes produced in Belgium may contain plastic and rubber pieces. This could cause choking or injury if eaten. Affected products have specific lot numbers listed in the recall. Read more at govinfonow.com/recall/18644-lutosa-plain-mashed-potatoes-recall-foreign-plastic-rubber-pieces-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/18644-lutosa-plain-mashed-potatoes-recall-foreign-plastic-rubber-pieces-risk · Updated October 6, 2026 · FDA enforcement record: FDA #F-0057-2019
Cite this page
“Lutosa Plain Mashed Potatoes Recall: Foreign Plastic/Rubber Pieces Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18644-lutosa-plain-mashed-potatoes-recall-foreign-plastic-rubber-pieces-risk. Based on FDA recall #F-0057-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0057-2019%22&limit=1).
Why it’s dangerous
The product may contain small plastic and rubber pieces that could be ingested. If swallowed, these pieces could cause choking or internal injury. The hazard is not immediate but could occur during consumption.
Who’s affected
Anyone who purchased Lutosa Foodservice Quality Plain Mashed potatoes from Belgium with the listed lot numbers. Children and those with swallowing difficulties are at slightly higher risk.
How to tell if you have this one
Check the lot numbers on the packaging: L8056 24 20, L8057 24 14, L8057 24 15, L8057 24 16, L8057 24 17, L8057 24 18, or L8057 24 19. The product is a 2.5 kg/5.5 lb plain mashed potato product from Belgium.
- Brand
Lutosa- Category
Food
What to do — step by step
Check Product Lot Numbers
Look for lot numbers L8056 24 20, L8057 24 14, L8057 24 15, L8057 24 16, L8057 24 17, L8057 24 18, or L8057 24 19 on the packaging.
Where it went and when
Where it was distributed
Distributed in Nevada, and outside the U.S.
FDA distribution: “U.S. distribution to NV. Foreign distribution to Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Nevada.
Recall timeline
FDA terminated this recall 7 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-0057-2019 (September 24, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0057-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.