CLASS I Food recall · Reported 26 Jun 2013 · FDA Enforcement Report

vega one, all-in one nutrition bar recalled by Sequel Naturals

Sequel Naturals is recalling vega one, all-in one nutrition bar, distributed nationwide in the US. The recall was initiated on 7 Jun 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot code: 13026U 14-Feb
Quantity recalled1328 boxes, 808 singles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1547-2013
FDA event ID
65412
Recalling firm
Sequel Naturals, Port Coquitlam
Classification
Class I
Status
Terminated
Recall initiated
7 Jun 2013
FDA classified
20 Jun 2013
Reported
26 Jun 2013
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Probiotics

Timeline

7 Jun 2013Recall initiated by company
20 Jun 2013Classified by FDA+13 days
26 Jun 2013Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

vega one, all-in one nutrition bar; Double chocolate 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:838766070032

Where it was distributed

Nationwide distribution.

Nationwide

Questions about this recall

Is vega one, all-in one nutrition bar recalled?

Yes. Sequel Naturals recalled vega one, all-in one nutrition bar on 7 Jun 2013. The recall is Class I and its status is Terminated. Recall number F-1547-2013.

Why was it recalled?

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

Which lots are affected?

Lot code: 13026U 14-Feb

Where was it sold?

Nationwide distribution.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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