FDA recall record

Dreyers Grand Ice Cream Outshine Fruit & Cream Bars - Creamy Pineapple Coconut 6 fruit recall — FDA F-0192-2021

Firm received complaints of foreign material in ice cream bars.

Class IIclassification
F-0192-2021official record ID
Dec 23, 2020report date

Recall record at a glance

Official recordF-0192-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDreyers Grand Ice Cream, Inc.
Report dateDec 23, 2020
Recall initiation dateDec 11, 2020
Quantity856 Cases
LocationOakland, CA, United States

Official product description

Outshine Fruit & Cream Bars - Creamy Pineapple Coconut 6 fruit and dairy bars, 14.7 fl. oz. UPC: 41548 91817 4 Distributed by Nestle Dreyers Ice Cream, Oakland, CA

Why the product was recalled

Firm received complaints of foreign material in ice cream bars.

Distribution information

MA, MI, NH, PA, VT.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.