Recall record at a glance
| Official record | F-2439-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bulletproof 360 Inc. |
| Report date | Jul 12, 2017 |
| Recall initiation date | Jun 14, 2017 |
| Quantity | 6,421 boxes (or 80,341 bars) |
| Location | Bellevue, WA, United States |
Official product description
Vanilla Shortbread Collagen Protein Bar. Each Bar is packed in foil wrapper, net wt. per Bar is 1.58 oz (45g). There 12 bars packed in a box and the net wt. is 18.96 oz (540g). Individual Bar UPC 815709021481. Box UPC 815709020804.
Why the product was recalled
Vanilla Shortbread Collagen Protein Bar product is recalled because it has the potential to be contaminated with Listeria monocytogenes.
Distribution information
nationwide including Puerto Rico, U.S. Virgin Islands, and sold online at bulletproof.com. Products were distributed internationally in the following countries: Australia, Bahrain, Bermuda, Bolivia, Brazil, Brunei Darussalam, Canada, Cayman Islands, China, Finland, France, Germany, Guam, Hong Kong, Hungary, Iceland, Israel, Japan, Korea, Kuwait, Liechtenstein, Macau, Malaysia, Malta, Mexico, Monaco, Netherlands, New Zealand, Norway, Oman, Philippines, Romania, Saudi Arabia, Singapore, Spain, Switzerland, Taiwan, United Arab Emirates, 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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