Abby's Best BISCUIT MIX recall
Recalled by Alfa Supply, Inc. · Hanahan, SC, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
During an inspection by the SCDA the firm was notified that their label does not declare the allergen wheat.
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
Abby's Best BISCUIT MIX NET WEIGHT 4 LBS. 8 OZ. (2.04 KG) INGREDIENTS: ENRICHED BLEACHED FLOUR***PARTIALLY HYDROGENATED VEGETABLE SHORTENING (CONTAINS SOYBEAN OIL) WITH EMULSIFIER***LEAVENING***BUTTERMILK, SALT, SUGAR, CALSIUM CARBONATE PACKED FOR ABBY'S BEST BY ALFA MANUFACTURING CHARLESTON, SC 29406
Quantity: 877cs/6/4lb 8oz cans
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.
Lot numbers embossed on top of the cans: 07524, 09524, 10724, 13424, 14224, 14924, 15124, 17024, 17324 & 17824.
Where it was sold
California Florida Virginia Washington
FDA's distribution note: Product was shipped to the following states: CA, FL. VA & WA. Product was also sent to the country of Bahrain.
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 completed: 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
- Alfa Supply, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 1, 2024
- In FDA report of
- Aug 21, 2024
- FDA recall number
- F-1706-2024 · event 94911
- Official record
- FDA enforcement report search