Recalled by Epic Enterprises, Incorporated · Ayer, MA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Product contains undeclared sweetener - aspartame
See the recall's own reason text for the specifics. All other reasons recalls.
Dr. Pepper 24 pack of 12 FL OZ Cans (288 FL OZ) in cardboard cases: Produced under the authority of Dr. Pepper/Seven Up, Inc., 5301 Legacy Drive, Plano, TX 75024; Best Before: JUN 29 20; Case UPC: 078000082104; Can UPC: 07831504
Quantity: 1703 cases
Food: Spices & seasonings
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Outer wrap Dates: Ship To Satelite 03/09/2020; Ship To Trade 05/18/2020; Best Taste Before 06/29/2020 Case date: JUN 29 20 Case Lot: XXXXEA09239CD Can date: JUN 29 20 Can Lot: XXXXEA09239C
Connecticut Maine Rhode Island
FDA's distribution note: Products were distributed in CT, ME, RI
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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.
Reason Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.
Reason Salmonella. The firm received a positive test result of Salmonella in the product.
Reason Potential contamination with Salmonella.
Reason Product tested positive for undeclared milk allergen.