Recall record at a glance
| Official record | F-2404-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bounce Life Style HQ |
| Report date | Oct 5, 2016 |
| Recall initiation date | Jun 8, 2016 |
| Quantity | 80,701 loose bars distributed in UK |
| Location | Bend, OR, United States |
Official product description
Bounce Energy Ball Cashew & Pecan Vitality Lift, each loose unit has net wt 42 gram. The bulk pack (contains 60 pieces) has UPC 9335805000872 and 9335805000308. The jar (contains 40 pieces) has UPC 9335805000254. Bounce Energy Ball Cashew & Pecan Vitality Lift unit has UPC 9335805000094 (61,764 balls); 9335805001077 (7,200 balls); and 9335805000049 (257 balls).
Why the product was recalled
Bounce Energy Ball Cashew & Pecan Vitality Lift is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product contains sunflower kernels that were recalled by supplier SunOpta.
Distribution information
distributed nationwide in the US and in Australia, Canada, and United Kingdom.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.