FDA Recall United States Terminated Historical recordClass II
Abbott Laboratories
- Product
- Pedialyte with Immune Support***+Zinc/Selenium & Magnesium**…
- Published
- June 29, 2022
- Distribution
- AL, AR, AZ, CA, CO, DE, FL, GA, IA, IL,…
Abbott Laboratories Recall: These products are being recalled due to the potential of leakage from the 1L container.
United States
TerminatedClass II
- Company
- Abbott Laboratories
- Product
- Pedialyte with Immune Support***+Zinc/Selenium & Magnesium**…
- Recall date
- June 3, 2022
- Terminated
- April 14, 2023
- Source
- FDA
Reason for recall
These products are being recalled due to the potential of leakage from the 1L container.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Pedialyte 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 | Not published in this source record | 50,502 (2-count cases) | 30295SG00, 30296SG00, 30297SG00, 30298SG00, 30299SG00, 35415SG00, 35416SG00, 35417SG00, 35418SG00, 38452SG00, 38453SG00 and 38454SG00. |
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
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1343-2022
- Event ID
- 90379
- Status
- Terminated
- Classification
- Class II
- Company
- Abbott Laboratories
- Product description
- Pedialyte 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
- Quantity
- 50,502 (2-count cases)
- Reason
- These products are being recalled due to the potential of leakage from the 1L container.
- Recall initiation date
- June 3, 2022
- Report date
- June 29, 2022
- Classification date
- Not published in this source record
- Termination date
- April 14, 2023
- Distribution pattern
- 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
- UPC, lot, and code information
- 30295SG00, 30296SG00, 30297SG00, 30298SG00, 30299SG00, 35415SG00, 35416SG00, 35417SG00, 35418SG00, 38452SG00, 38453SG00 and 38454SG00.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 90379 with 1 other product entry in Public Health Trace.
Responsible company: Abbott Laboratories
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- Product
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- Published
- November 15, 2023
- Distribution
- Alabama, Arkansas, Arizona, California,…
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- Published
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- Distribution
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- Product
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- Published
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- Distribution
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A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Delaware | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Michigan | 1 |
| Missouri | 1 |
| Mississippi | 1 |
| North Carolina | 1 |
| New Hampshire | 1 |
| New York | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
