Recall record at a glance
| Official record | F-0418-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | 1 Epic, LLC |
| Report date | Nov 16, 2016 |
| Recall initiation date | Oct 18, 2016 |
| Quantity | 5,832 cases (24 cans per cases) |
| Location | Gilbert, AZ, United States |
Official product description
Fruit 66 Passion Fruit Mango, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other natural Flavors and added Ingredients. UPC 98341-00109.
Why the product was recalled
1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice products because the cans are experiencing swelling that can cause the lids of the can to pop off and potentially cause an injury.
Distribution information
AL, CA, FL, GA, IL, KY, MD, MI, NY, OH, PA, TN, TX, VA.
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.