Meduri Farms Dried Strawberries Recall: Peanut Contamination Risk
Meduri Farms recalls dried strawberries with sugar infusion due to peanut contamination on packaging line. Affected products include 10-25lb boxes with lot codes 22818067208 and 23086067205.
Lower-risk recall
Meduri Farms Dried Strawberries/Sugar Infused product is being recalled because half of a peanut was found on the packaging line.
Contact the company
What happened, in plain English
Meduri Farms is recalling dried strawberries with sugar infusion because a peanut was found on the packaging line. This contamination could pose a risk to people with peanut allergies. Read more at govinfonow.com/recall/21122-meduri-farms-dried-strawberries-recall-peanut-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/21122-meduri-farms-dried-strawberries-recall-peanut-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2473-2017
Cite this page
“Meduri Farms Dried Strawberries Recall: Peanut Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21122-meduri-farms-dried-strawberries-recall-peanut-contamination-risk. Based on FDA recall #F-2473-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2473-2017%22&limit=1).
Why it’s dangerous
The product was found to have a peanut on the packaging line during production. This could lead to peanut contamination in the product, which is dangerous for individuals with peanut allergies.
Who’s affected
People who purchased Meduri Farms dried strawberries with sugar infusion in 10-25lb boxes or 10kg packages with lot codes 22818067208 or 23086067205 are affected. Those with peanut allergies are at higher risk.
How to tell if you have this one
Check for the product name 'Meduri Farms Dried Strawberries/Sugar Infused' with catalog number 010282. Look for lot codes 22818067208 or 23086067205 on the packaging.
- Brand
Meduri Farms- Category
Food
What to do — step by step
Check Product Label
Look for the lot codes 22818067208 or 23086067205 on the packaging to confirm if the product is affected.
Where it went and when
Where it was distributed
Distributed in California, and outside the U.S.
FDA distribution: “California and Canada” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA terminated this recall 21 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-2473-2017 (June 7, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2473-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.