FindMyRecallSubscribe
Class III: unlikely to cause harmTerminated

Abbott Laboratories Pedialyte***Replaces Electrolytes***Great Recall

Pedialyte***Replaces Electrolytes***Great for Kids and Adults***Strawberry Lemonade Nat…

Abbott Laboratories · Columbus, OH

Risk level
Class III
Reported by FDA
Jun 22, 2022
Recall ID
F-1312-2022
Check your lot numberHow we source this data

Summary

Abbott Laboratories recalled Pedialyte***Replaces Electrolytes***Great starting Jun 3, 2022. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1312-2022 on Jun 22, 2022. Reason: 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. Status: Terminated.

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.

Product description

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

Lot numbers, UPCs & expiration codes

287112S00

Where it was sold

AZ, CA, FL, GA, IL, IN, MN, NC, NY, OH, KS, and TN.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1312-2022
Classification
Class III
Status
Terminated
Recall initiated
Jun 3, 2022
FDA report date
Jun 22, 2022
Quantity
789 cases/4734 cartons/28,404 packets
Recall type
Voluntary: Firm initiated
Recalling firm
Abbott Laboratories

Original FDA data

Every field from FDA enforcement report F-1312-2022, exactly as published.

Show all FDA fields
City
Columbus
State
OH
Status
Terminated
Country
United States
Event ID
90385
Address
2900 Easton Square Pl
Code information
287112S00
Postal code
43219-6225
Report date
Jun 22, 2022
Product type
Food
Recall number
F-1312-2022
Classification
Class III
Recalling firm
Abbott Laboratories
Product quantity
789 cases/4734 cartons/28,404 packets
Termination date
Dec 21, 2022
Reason for recall
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
AZ, CA, FL, GA, IL, IN, MN, NC, NY, OH, KS, and TN.
Recall initiation date
Jun 3, 2022
Initial firm notification
Letter
Center classification date
Jun 15, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1312-2022, published Jun 22, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls