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Lower risk Food recall · FDA · Published June 3, 2022

Abbott Pedialyte with Immune Support: Potential Leakage Risk

Abbott recalls Pedialyte with Immune Support due to potential leakage from the 1L container. This may cause spills or contamination. Consumers should check product codes and contact Abbott for details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #F-1343-2022FoodAbbott ›
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Contact the company

Recalling firmAbbott Laboratories2900 Easton Square Pl · Columbus, OH 43219-6225
✎ GovInfoNow plain-language explainer

Abbott is recalling Pedialyte with Immune Support because the 1L container might leak. This could lead to spills or contamination of the product, especially if the container is not properly sealed. Read more at govinfonow.com/recall/12723-abbott-pedialyte-with-immune-support-potential-leakage-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/12723-abbott-pedialyte-with-immune-support-potential-leakage-risk · Updated October 4, 2026 · FDA enforcement record: FDA #F-1343-2022

Cite this page

“Abbott Pedialyte with Immune Support: Potential Leakage Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/12723-abbott-pedialyte-with-immune-support-potential-leakage-risk. Based on FDA recall #F-1343-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1343-2022%22&limit=1).

Abbott Laboratories voluntarily recalled Pedialyte with Immune Support Peach Mango flavor, 33.8 FL OZ containers due to potential leakage from the 1L container, according to the FDA on June 3, 2022.

How to tell if you have it

  • Brand: Abbott
  • Product: Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05 QT) 1L
  • Lot codes: 30295SG00, 30296SG00, 30297SG00, 30298SG00, 30299SG00, 35415SG00, 35416SG00, 35417SG00, 35418SG00, 38452SG00, 38453SG00 and 38454SG00
  • Quantity: 50,502 (2-count cases)
  • 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

The hazard

These products are being recalled due to the potential of leakage from the 1L container.

Context

GovInfoNow's records show Abbott Laboratories has 33 other recalls on record since May 14, 2012. Other recent recalls include Abbott Alinity hq Analyzer Software Issue (March 18, 2025) and Abbott CELL-DYN Ruby: Expired Reagents Cause Incorrect Date Updates (March 18, 2025).

How to tell if you have this one

Check the product code on the label, which includes numbers like 30295SG00 to 38454SG00. These products were sold in the U.S. and are labeled with the specific container size.

  • Brand
    Abbott
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • 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
Recall numberProduct, codes & lotsQuantity
F-1343-2022Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Peach Mango Natural & Artificial Flavor, 33.8 FL OZ (1.05 QT) 1L***INGREDIENTS: WATER, DEXTROSE*** Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219-3034 USA; 30295SG00, 30296SG00, 30297SG00, 30298SG00, 30299SG00, 35415SG00, 35416SG00, 35417SG00, 35418SG00, 38452SG00, 38453SG00 and 38454SG00.50,502 (2-count cases)
F-1344-2022Pedialyte 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; 30289SG00, 30290SG00, 30291SG00, 30292SG00, 30293SG00, 30294SG00, 35409SG00, 35410SG00, 35411SG00, 35412SG00, 36435SG00, 36434SG00, 36433SG00, 36432SG00, 37444SG00, 37443SG00, 37442SG00, 37441SG00, 37440SG00, and 41129D500.121,918 (2-count cases)
Based on the official FDA remedy

What to do — step by step

  1. Check Product Code

    Look for the product code on the label, which includes numbers like 30295SG00 to 38454SG00.

Where it went and when

Where it was distributed

Distributed in 28 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: yesNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: yesDEArizona: yesAZNew Mexico: not listedNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA 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 read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, Arkansas, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Michigan, Mississippi, Missouri, New Hampshire, New York, North Carolina, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia, Wisconsin.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Jun 3, 202212. FDA classified it Class II: Jun 22, 202223. Published in FDA’s Enforcement Report: Jun 29, 202234. FDA terminated the recall: Apr 14, 2023420222023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-1343-2022 (June 3, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1343-2022 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA