Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in…
Dreyer's Grand Ice Cream Inc. recalled this product and the FDA reported the enforcement action on 2 September 2026 as Class II. The recall was initiated by the firm. Foreign object: products may contain glass pieces
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
- UPC
- 041548610047
- Reason for recall
- Foreign object: products may contain glass pieces
- Recalling firm
- Dreyer's Grand Ice Cream Inc.
- Firm location
- Laurel, Maryland, United States
- Classification
- Class II
- Status
- Ongoing
- Recall number
- H-1264-2026
- Quantity
- 644 pallets
- Distribution
- 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.
- Initiated
- 18 August 2026
- Reported by FDA
- 2 September 2026
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Batch code/ Best Before (bottom of package): LLA616903 30 SEP 2027 LLA617003 30 SEP 2027 LLA617103 30 SEP 2027 LLA617203 30 SEP 2027 LLA617303 30 SEP 2027 LLA617403 30 SEP 2027 LLA617503 30 SEP 2027 LLA617603 30 SEP 2027 LLA620303 31 OCT 2027 LLA620403 31 OCT 2027 LLA620503 31 OCT 2027 LLA620603 31 OCT 2027 LLA620703 31 OCT 2027 LLA620803 31 OCT 2027 LLA620903 31 OCT 2027 LLA621003 31 OCT 2027 LLA621103 31 OCT 2027 LLA621203 31 OCT 2027 LLA621303 30 NOV 2027 LLA621403 30 NOV 2027 LLA621503 30 NOV 2027 LLA621603 30 NOV 2027
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 6 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 6 separate recalls, which almost every published figure does, overstates it by a factor of 6. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 6 of them.
- This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
- The distribution pattern names 31 states, and the FDA published the enforcement report 2 weeks after the firm began the recall.
- Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: 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, Utah, Virginia, U.S. Virgin Islands, Washington, Wisconsin. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Foreign material
A foreign material recall means something that is not food was found in food: metal, plastic, glass, wood or insect matter, usually shed by equipment during processing.
A preventive controls plan covers foreign material under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.40
- Equipment and utensils: plant equipment designed and maintained so it cannot contaminate food with lubricants, fuel, metal fragments or contaminated water.
- 21 CFR 117.80(c)
- Manufacturing operations: the measures that protect food from contamination during processing, including the effective ones against metal and other extraneous material.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Filed under fresh produce. A product can sit in more than one.
Other fresh produce recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Dreyer's Grand Ice Cream Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 7 other records name this firm.
All 8 records for Dreyer's Grand Ice Cream Inc.
All 2026 recalls · All FDA food recall data
21 CFR 117.40 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.