Marlyce's Homemade Butterballs
Reason Undeclared allergens. The product label does not declare allergens of Wheat Flour, Soy Flour, Whey, and Milk.
Marlyce's Homemade Style Noodles recall
Recalled by L. M. Noodle Company, LLC · Wiggins, CO, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
L.M. Noodle Company is recalling Marlyce's Homemade Style Noodles due to an undeclared allergen. The product label does not declare "wheat" flour.
Undeclared allergen: Wheat
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
Marlyce's Homemade Style Noodles, Net Wt. 8 oz, Packaged in plastic bags, 10 per case, UPC 094219217069. Manufactured by L.M.Noodle Company, LLC, 416 Main Street, Wiggins, CO 80654.
Quantity: 18,200
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.
UPC 094219217069,
Where it was sold
Colorado Nebraska Virginia Wyoming
FDA's distribution note: Product was distributed to retail stores in NE, CO, WY. No foreign, military/govt/VA consignees.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat; 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
- L. M. Noodle Company, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 20, 2013
- In FDA report of
- Mar 5, 2014
- Terminated
- Mar 10, 2014
- FDA recall number
- F-1559-2014 · event 67579
- Official record
- FDA enforcement report search
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