Outshine Fruit Bars Black Cherry recall

Recalled by Dreyer's Grand Ice Cream Inc. · Laurel, MD, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Foreign object: products may contain glass pieces

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.

Quantity: 226 pallets

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Batch code/ Best Before (bottom of package): LLA618503 31 JUL 2027 LLA618603 31 JUL 2027 LLA618703 31 JUL 2027 LLA618803 31 JUL 2027 LLA618903 31 JUL 2027 LLA619003 31 JUL 2027

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Iowa Idaho Illinois Kansas Louisiana Massachusetts Maryland Michigan Minnesota Missouri North Carolina North Dakota New Hampshire New Jersey Nevada New York Ohio Pennsylvania Puerto Rico Tennessee Texas Utah Virginia Washington Wisconsin

FDA's distribution note: 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.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.

Recalling firm: Dreyer's Grand Ice Cream Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Aug 18, 2026
In FDA report of: Sep 2, 2026
FDA recall number: H-1268-2026 · event 99716
Official record: FDA enforcement report search

Also recalled with it (5 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Ongoing Foreign material Aug 18, 2026