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Class ITerminated in FDA datasetRecall initiated Jun 7, 2013

vega one, all-in one nutrition bar; chocolate cherry flavor Added vitamins and minerals; 15 g…

Recalling firm: Sequel Naturals Ltd

Why it was recalled

Raw material supplier of the chocolate used for the bar coating had milk ingredients added inadvertently. One report of ampholytic reaction.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 28, 2013.

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Compare the exact product and package details with the label you have.

Productvega one, all-in one nutrition bar; chocolate cherry flavor Added vitamins and minerals; 15 g Protein, 6 g Fiber and 1.5 g Omega Antioxidants, probiotics & greens; Gluten Free Dietary Supplement. 2.2 oz/ 63g Made in a facility that processes peanuts, tree nuts, sesame, dairy, and soy. May contain fruit shell or nut pieces. Distributed by Sequels Naturals LTD, Burnaby, BC, Canada UPC: 838766070056
Package size15 g
UPC838766070056

FDA code information

Lot code: 13032U, 14-Mar

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Full FDA record and distribution details

Original product description

vega one, all-in one nutrition bar; chocolate cherry flavor Added vitamins and minerals; 15 g Protein, 6 g Fiber and 1.5 g Omega Antioxidants, probiotics & greens; Gluten Free Dietary Supplement. 2.2 oz/ 63g Made in a facility that processes peanuts, tree nuts, sesame, dairy, and soy. May contain fruit shell or nut pieces. Distributed by Sequels Naturals LTD, Burnaby, BC, Canada UPC: 838766070056

Extracted codes and context

TypeCode / valueContext
UPC838766070056 or nut pieces. Distributed by Sequels Naturals LTD, Burnaby, BC, Canada UPC: 838766070056
lot13032ULot code: 13032U, 14-Mar
lot14-MarLot code: 13032U, 14-Mar

Original FDA recall reason

Raw material supplier of the chocolate used for the bar coating had milk ingredients added inadvertently. One report of ampholytic reaction.

Recall details

Recall number
F-1546-2013
Event ID
65412
FDA status
Terminated
Initiated
Jun 7, 2013
Reported
Jun 26, 2013
Classified
Jun 20, 2013
Terminated
Oct 28, 2013
Quantity
1292 boxes, 2734 singles
Location
Port Coquitlam, Canada
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide distribution.

FDA source record · F-1546-2013

Data updated September 16, 2026. View official FDA data ↗

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