Recall record at a glance
| Official record | F-0771-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | CHOBANI |
| Report date | Feb 14, 2018 |
| Recall initiation date | Jan 17, 2018 |
| Quantity | 84,748 cases (3 packs per cases) |
| Location | Norwich, NY, United States |
Official product description
Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz cups are packaged with a cardboard overwrap. The net wt. of each single serve up is 5.3 oz. and the net wt. of 4-pack is 21.2 oz. The 4-pack overwrap label has the UPC 8 18290 01484 9 and single serve cup has the UPC 8 18290-01227 2.
Why the product was recalled
Product is recalled because a statement on the overwrap label erroneously states "No Gluten" while the ingredients statement and the Contains statements on both the overwrap label and the flip label on each individual cup declare wheat.
Distribution information
distributed in AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WY, including Puerto Rico.
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.