Food Recall Check
Class III · Low risk Terminated Initiated Jun 3, 2022 (4 years ago)

Pedialyte***Replaces Electrolytes***Great for Kids and… recall

Recalled by Abbott Laboratories · Columbus, OH, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

The third party contract manufacturer used a dextrose ingredient derived from wheat in one lot of the Strawberry Lemonade powder, which is not declared on the label.

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

Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry Lemonade Natural Flavor with Other Natural Flavor*** 6 0.6 OZ (17g) PACKETS/NET WT. 3.6 OZ (102g)***INGREDIENTS: ANHYDROUSE DEXTROSE, CITRIC ACID, POTASSIUM CITRATE***Manufactured for: Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219

Quantity: 789 cases/4734 cartons/28,404 packets

Food: Berries Juice & beverages

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.

287112S00

Where it was sold

Arizona California Florida Georgia Illinois Indiana Kansas Minnesota North Carolina New York Ohio Tennessee

FDA's distribution note: AZ, CA, FL, GA, IL, IN, MN, NC, NY, OH, KS, and TN.

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. 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
Abbott Laboratories
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 3, 2022
In FDA report of
Jun 22, 2022
Terminated
Dec 21, 2022
FDA recall number
F-1312-2022 · event 90385
Official record
FDA enforcement report search

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Abbott Laboratories 41 states F-0328-2024

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Class II · Moderate risk Ongoing Foreign material

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