Class IIOngoing in FDA datasetRecall initiated Aug 18, 2026

Outshine Fruit Bars Grape

Recalling firm: Dreyer's Grand Ice Cream Inc.

Why it was recalled

Foreign object: products may contain glass pieces

Check your package

Compare the exact product and package details with the label you have.

ProductOutshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Package size2.5 ounce
UPC041548244044

FDA code information

Batch code/ Best Before (bottom of package): LLA616803 30 SEP 2027 LLA616903 30 SEP 2027 LLA619703 31 OCT 2027 UPC Bottom of package: 041548244044 LLA619803 31 OCT 2027 LLA619903 31 OCT 2027 LLA620003 31 OCT 2027 LLA620103 31 OCT 2027 LLA620203 31 OCT 2027 LLA620303 31 OCT 2027

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Full FDA record and distribution details

Original product description

Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Extracted codes and context

TypeCode / valueContext
UPC041548244044Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, 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-1266-2026
Event ID
99716
FDA status
Ongoing
Initiated
Aug 18, 2026
Reported
Sep 2, 2026
Classified
Aug 26, 2026
Quantity
281 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.

FDA source record · H-1266-2026

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.