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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Food & Beverages/Baby Food & Formula

Pedialyte Strawberry Lemonade Recalled for Undeclared Wheat

Agency Publication Date: June 15, 2022
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Summary

Abbott Laboratories is recalling 789 cases (approximately 28,404 packets) of Pedialyte Strawberry Lemonade powder packets. A contract manufacturer used a dextrose ingredient derived from wheat that was not listed on the product label. No incidents or injuries have been reported to date. Consumers who purchased the affected packets should check for lot number 287112S00 and return the product to the place of purchase for a refund or dispose of it.

Risk

Individuals with a wheat allergy or severe sensitivity to wheat risk a serious or life-threatening allergic reaction if they consume this product.

What You Should Do

  1. This recall involves Pedialyte Strawberry Lemonade electrolyte powder packets sold in 3.6 oz cartons containing six 0.6 oz packets. Affected products are identified by lot number 287112S00.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact the manufacturer for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions or concerns regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Pedialyte Strawberry Lemonade (3.6 oz)
Variants: Strawberry Lemonade Natural Flavor, 6 Packets (0.6 oz each)
Lot Numbers:
287112S00

Recall number: F-1312-2022. Quantity affected: 789 cases/4734 cartons/28,404 packets.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90385
Status: Resolved
Manufacturer: Abbott Laboratories
Sold By: Retailers in distribution states
Manufactured In: United States
Units Affected: 789 cases/4734 cartons/28,404 packets
Distributed To: Arizona, California, Florida, Georgia, Illinois, Indiana, Minnesota, North Carolina, New York, Ohio, Kansas, Tennessee

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.