Whitley's Peanut Factory recall
Recalled by Whitley Peanut Factory, Inc. · Hayes, VA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared Allergen (peanuts, milk, soy, wheat, and sesame).
Undeclared allergens: Milk Peanut Soy Wheat Sesame
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
Whitley's Peanut Factory, Deluxe Nut Mix, 12oz (340g), Electrolytic tin-plated cans, with paper label. 12-pack case boxes.
Quantity: 840.75 pounds
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: 703795000551, Lot Codes: MFG 22823; MFG 25023; MFG 25823. MFG 29323; MFG 35623
Where it was sold
Alabama Arizona California Colorado Connecticut Delaware Florida Georgia Iowa Illinois Kentucky Massachusetts Maryland Michigan Minnesota Missouri Montana North Carolina Nebraska New Jersey New York Ohio Pennsylvania South Carolina Tennessee Texas Virginia Washington
FDA's distribution note: The recalled product was distributed to the following states: NY, PA, DE, VA, FL, OH, NC, NE, CO, AL, KY, MN, CA, TN, CT, WA, MA, IL, HN, NY, NJ, SC, MO, IA, GA, TX, AZ, MT, MD, MI, IA and NJ
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, peanut, soy, wheat, sesame; 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
- Whitley Peanut Factory, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 18, 2024
- In FDA report of
- Apr 17, 2024
- Terminated
- May 23, 2024
- FDA recall number
- F-1129-2024 · event 93841
- Official record
- FDA enforcement report search