CLASS I Food recall · Reported 24 Sep 2014 · FDA Enforcement Report

Green Vibrance serve pkts recalled by Vibrant Health

Vibrant Health is recalling Green Vibrance serve pkts, distributed nationwide in the US. The recall was initiated on 25 Jul 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot Number: 1401076
Quantity recalled8,726

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-2435-2014
FDA event ID
68949
Recalling firm
Vibrant Health, Canaan, CT
Classification
Class I
Status
Terminated
Recall initiated
25 Jul 2014
FDA classified
12 Sep 2014
Reported
24 Sep 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Salmonella
Product category
Fish

Timeline

25 Jul 2014Recall initiated by company
12 Sep 2014Classified by FDA+49 days
24 Sep 2014Published in enforcement report+12 days

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

Reason for recall

A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Green Vibrance 15 single serve pkts, 181.5g, 6.4oz. Product Code: GVSD

Where it was distributed

Nationwide OUS: UK, Iceland, South Africa

Nationwide

Questions about this recall

Why was it recalled?

A raw material used in the manufacture of the dietary supplements was found to contain Salmonella bacteria.

Which lots are affected?

Lot Number: 1401076

Where was it sold?

Nationwide OUS: UK, Iceland, South Africa

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

Other products in this recall event

3 other products · FDA event 68949

This product is part of a recall event; the main page for the event is Green Vibrance- A Comprehensive Restorative Advanced Daily recalled.

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