Outshine Fruit Bar Watermelon
Recalling firm: Dreyer's Grand Ice Cream Inc.
Foreign object: products may contain glass pieces
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Compare the exact product and package details with the label you have.
041548413624Batch codes & best-before dates
| Batch code | Best before |
|---|---|
LLA617603 | 30 JUN 2027 |
LLA617703 | 30 JUN 2027 |
LLA617803 | 30 JUN 2027 |
LLA617903 | 30 JUN 2027 |
LLA618003 | 30 JUN 2027 |
LLA618103 | 30 JUN 2027 |
| Batch code | Best before |
|---|---|
LLA618203 | 31 JUL 2027 |
LLA618303 | 31 JUL 2027 |
LLA618403 | 31 JUL 2027 |
LLA618503 | 31 JUL 2027 |
LLA619003 | 31 JUL 2027 |
LLA619103 | 31 JUL 2027 |
LLA619203 | 31 JUL 2027 |
LLA619303 | 31 JUL 2027 |
LLA619403 | 31 JUL 2027 |
LLA619503 | 31 JUL 2027 |
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Original FDA code information
Batch code/ Best Before (bottom of package): LLA617603 30 JUN 2027 LLA617703 30 JUN 2027 LLA617803 30 JUN 2027 LLA617903 30 JUN 2027 LLA618003 30 JUN 2027 LLA618103 30 JUN 2027 LLA618203 31 JUL 2027 LLA618303 31 JUL 2027 LLA618403 31 JUL 2027 LLA618503 31 JUL 2027 LLA619003 31 JUL 2027 LLA619103 31 JUL 2027 LLA619203 31 JUL 2027 LLA619303 31 JUL 2027 LLA619403 31 JUL 2027 LLA619503 31 JUL 2027
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 041548413624 | Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder. |
Original FDA recall reason
Foreign object: products may contain glass pieces
Recall details
- Recall number
- H-1265-2026
- Event ID
- 99716
- FDA status
- Ongoing
- Initiated
- Aug 18, 2026
- Reported
- Sep 2, 2026
- Classified
- Aug 26, 2026
- Quantity
- 685 pallets
- Location
- Laurel, MD, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
The adulterated product was distributed to the following States: AL, AR, AZ, CA,CO,CT, FL,GA, IA,ID, IL, KS, LA, MA,MD,MI, MN,MO, NC, ND, NH, NJ, NV, NY, OH, PA, PR, TN TX, UT, VA, VI, WA, and WI.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.