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.
Reported: July 12, 2017 Initiated: June 14, 2017 #F-2439-2017
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.
Reason for Recall
Vanilla Shortbread Collagen Protein Bar product is recalled because it has the potential to be contaminated with Listeria monocytogenes.
Details
- Recalling Firm
- Bulletproof 360 Inc
- Units Affected
- 6,421 boxes (or 80,341 bars)
- Distribution
- 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.
- Location
- Bellevue, WA
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Bulletproof 360 Inc. Units affected: 6,421 boxes (or 80,341 bars).
Why was this product recalled? ▼
Vanilla Shortbread Collagen Protein Bar product is recalled because it has the potential to be contaminated with Listeria monocytogenes.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on July 12, 2017. Severity: Critical. Recall number: F-2439-2017.
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