Recall record at a glance
| Official record | H-0300-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | DANONE US LLC |
| Report date | Jul 23, 2025 |
| Recall initiation date | Jul 11, 2025 |
| Quantity | 2,492,073 cases (total) |
| Location | White Plains, NY, United States |
Official product description
YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis candies, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00083 2. Multipack containing 4-4 oz. cups UPC 46675-01312 Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605
Why the product was recalled
Foreign material (plastic pieces)
Distribution information
Nationwide
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: E-Mail.
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.