Abbott recalls Pedialyte Strawberry Lemonade powder due to unlabeled wheat-derived dextrose in one lot. This may cause allergic reactions for those with wheat allergies. Consumers should check product codes and contact Abbott for details.
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.
“Abbott Pedialyte Strawberry Lemonade Powder Recall: Unlabeled Wheat Dextrose.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/12722-abbott-pedialyte-strawberry-lemonade-powder-recall-unlabeled-wheat-dextrose. Based on FDA recall #F-1312-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1312-2022%22&limit=1).
The FDA announced on June 3, 2022, that Abbott Laboratories is recalling Pedialyte Strawberry Lemonade powder because it contains undeclared wheat-derived dextrose. The agency issued recall number F-1312-2022 for the Class III voluntary recall.
How to tell if you have it
Brand: Abbott
Product: Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry Lemonade Natural Flavor with Other Natural Flavor
Size: 6 0.6 OZ (17g) packets/NET WT. 3.6 OZ (102g)
Lot code: 287112S00
Distribution: AZ, CA, FL, GA, IL, IN, MN, NC, NY, OH, KS, and TN
The hazard
According to the FDA, the third-party contract manufacturer used a dextrose ingredient derived from wheat in one lot of the Strawberry Lemonade powder. This allergen is not declared on the label.
Context
GovInfoNow's records show Abbott Laboratories has 33 other recalls on record since May 14, 2012. Recent Abbott recalls include an Alinity ci-series System Control Module correction announced on November 13, 2025, and a CELL-DYN Ruby reagent scanning hazard reported on March 18, 2025. Other recent recalls of similar products include Wawa Diet Lemonade P (April 2, 2026) and Meijer Vanilla Bourbon Trail Mix (April 21, 2026).
How to tell if you have this one
Check the product code on the packaging, which should be 287112S00 for the recalled batch. The product is labeled as 'Pedialyte Strawberry Lemonade Natural Flavor with Other Natural Flavor'.
Brand
Abbott
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Code
Look for the code 287112S00 on the packaging to identify the recalled batch.
Where it went and when
Where it was distributed
Distributed in 12 states.
Listed by the agency
Not listed
FDA distribution: “AZ, CA, FL, GA, IL, IN, MN, NC, NY, OH, KS, and TN.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Florida, Georgia, Illinois, Indiana, Kansas, Minnesota, New York, North Carolina, Ohio, Tennessee.
Recall timeline
FDA terminated this recall 7 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-1312-2022 (June 3, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1312-2022 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.