Recall archive / FDA food enforcement
Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry Lemonade Natural & Artificial Flavor, 33.8 FL ... — FDA record F-1344-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jun 3, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry Lemonade Natural & Artificial Flavor, 33.8 FL OZ (1.05 QT) 1L*** INGREDIENTS: WATER, DEXTROSE***Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219-3034 USA
- Reason
- These products are being recalled due to the potential of leakage from the 1L container.
- Classification
- Class II
- Recalling firm
- Abbott Laboratories
- Quantity
- 121,918 (2-count cases)
- Agency-reported status
- Terminated
- Source record identifier
- F-1344-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 30289SG00, 30290SG00, 30291SG00, 30292SG00, 30293SG00, 30294SG00, 35409SG00, 35410SG00, 35411SG00, 35412SG00, 36435SG00, 36434SG00, 36433SG00, 36432SG00, 37444SG00, 37443SG00, 37442SG00, 37441SG00, 37440SG00, and 41129D500. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
AL, AR, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MO, MS, NC, NH, NY, OH, OR, PA, TN, TX, UT, VA and WI
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Jun 29, 2022
- Recall initiation date
- Jun 3, 2022
- Center classification date
- Jun 22, 2022
- Termination date
- Apr 14, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.