Daily Chef Tropical Fruit & Nut Blend
Reason Undeclared ingredient; Yellow #5 & #6.
Walmart Great Value Tex Mex Trail Mix recall
Recalled by Ann's House of Nuts, Inc · Robersonville, NC, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains undeclared allergen; milk.
Undeclared allergen: Milk
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
Walmart Great Value Tex Mex Trail Mix, Net Wt 28 oz (793g), Distributed by Wal Mart Stores, Inc., Bentonville, AR, packed in rigid clear plastic jars.
Quantity: 55,717 cases (6/28 oz clear plastic jars per case)
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.
Best By date range: 04/18/2014 through 12/12/2014, UPC: 0 78742 03371 6
Where it was sold
Alabama Arkansas Arizona California Colorado Florida Georgia Illinois Kentucky Minnesota Missouri Mississippi North Carolina New Hampshire New York Pennsylvania Texas Virginia Washington
FDA's distribution note: AL, AR, AZ, CA, CO, FL, GA, IL, KY, MN, MO, MS, NC, NH, NY, PA, TX, VA, and WA.
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 milk; 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
- Ann's House of Nuts, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 20, 2013
- In FDA report of
- Feb 5, 2014
- Terminated
- Jan 25, 2017
- FDA recall number
- F-1464-2014 · event 67208
- Official record
- FDA enforcement report search