Mei Sh: 12oz Rice Noodles Recall - Undeclared Shrimp and Soybean Oil Hazard
Mei Shun Noodle Inc recalls 12oz rice noodles due to undeclared shrimp, soybean oil and green onions. Products may contain allergens without labeling. Consumers should check packaging for batch numbers.
Lower-risk recall
Undeclared shrimp, soybean oil and green onions in fresh rice noodles.
Contact the company
What happened, in plain English
Mei Shun Noodle Inc is recalling 12-ounce rice noodles because they contain undeclared shrimp, soybean oil, and green onions. This poses a risk for people with allergies to these ingredients who may not be aware of the allergens. Read more at govinfonow.com/recall/23440-mei-sh-12oz-rice-noodles-recall-undeclared-shrimp-and-soybean.
Source Summary by GovInfoNow · govinfonow.com/recall/23440-mei-sh-12oz-rice-noodles-recall-undeclared-shrimp-and-soybean · Updated October 9, 2026 · FDA enforcement record: FDA #F-0113-2017
Cite this page
“Mei Sh: 12oz Rice Noodles Recall - Undeclared Shrimp and Soybean Oil Hazard.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23440-mei-sh-12oz-rice-noodles-recall-undeclared-shrimp-and-soybean. Based on FDA recall #F-0113-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0113-2017%22&limit=1).
Why it’s dangerous
The noodles contain undeclared allergens that could cause allergic reactions in sensitive individuals. Since the ingredients are not listed on the packaging, people with allergies may unknowingly consume them.
Who’s affected
People with shrimp, soybean oil, or green onion allergies who consume the noodles are at risk. The recall affects consumers who bought the noodles from stores selling them in Chicago.
How to tell if you have this one
Check for 12-ounce rice noodles with a label from Mei Shun Noodle Inc in Chicago. The packaging does not have batch or lot numbers.
- Brand
Mei Shun Noodle Inc- Category
Food
What to do — step by step
Check Packaging
Look for the label from Mei Shun Noodle Inc on the packaging to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed in Illinois.
FDA distribution: “Illinois” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 3.4 years 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-0113-2017 (August 17, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0113-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.