The Hampton Grocer
Reason Product may be contaminated with Salmonella.
6 Five Rice Noodles recall
Recalled by Louis Hong Inc Dba Mei Shun Noodle Inc · Chicago, IL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared shrimp, soybean oil and green onions in fresh rice noodles.
Undeclared allergens: Soy Shellfish
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
6 Five, Rice Noodles, Keep Refrigerated, Ingredients: Rice flour, water, salt and corn oil. Weight: 12 oz, Manufactured by: Mei Shun Noodle Inc, 610 W. 26th Street Chicago IL 60613, (312) 842-6500. Noodles on styrofoam tray visible through clear plastic wrap.
Quantity: 60 packages
Food: Pasta, rice & grains
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
No batch, serial or lot numbers available on the packaging.
Where it was sold
Illinois
FDA's distribution note: Illinois
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to soy, shellfish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Louis Hong Inc Dba Mei Shun Noodle Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 17, 2016
- In FDA report of
- Oct 26, 2016
- Terminated
- Dec 30, 2019
- FDA recall number
- F-0113-2017 · event 75182
- Official record
- FDA enforcement report search
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