FDA recall record

Bounce Life Style HQ net wt recall — FDA F-2402-2016

Apple Cinnamon Protein Punch Energy Ball product is recalled because it has the potential to be contaminated with Listeria monocytogenes. This product…

Class Iclassification
F-2402-2016official record ID
Oct 5, 2016report date

Recall record at a glance

Official recordF-2402-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmBounce Life Style HQ
Report dateOct 5, 2016
Recall initiation dateJun 8, 2016
Quantity2450 cases in US; 223,252 loose packs in UK; 83,338 loose packs in Australia; 15,900 units in Canada
LocationBend, OR, United States

Official product description

US - Bounce Apple Cinnamon Protein Punch Energy Balls (old name), net wt. 1.48 oz. (42g). Product UPC Codes are 852949003723 (individual packs) and 852949003730 (12-unit boxes). US - Bounce Apple Cinnamon Protein Energy Balls (new name), net wt. 1.48 oz. (42g). Product UPC codes are 852949003723 (individual packs) and 852949003730 (12-unit boxes). Australia - Bounce Energy Ball Apple Cinnamon Protein Punch, individual pack has a net wt. 42g and UPC 19335805000374 and 40 pc. jar has UPC 9335805000469. Canada - Bounce Energy Ball Apple & Cinnamon Protein Punch, net wt. 42g, individual pack has UPC 852949003471. United Kingdom- Bounce Energy Ball Apple Cinnamon Protein Punch - individual pack has a net wt. 42g. The 60 pieces bulk pack has UPC 9335805000841;the 40 pieces jar has UPC 9335805000469; the 30 pieces tub has UPC 19335805000435; Other indiviual balls has UPCs 9335805000360; 9335805001060; 9335805001152; and 9335805000308. .

Why the product was recalled

Apple Cinnamon Protein Punch Energy Ball product 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

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