CLASS I Food recall · Reported 27 Aug 2014 · FDA Enforcement Report
Organic Carob Powder recalled by BrandStorm
BrandStorm is recalling Organic Carob Powder, distributed in North Dakota. The recall was initiated on 21 Jul 2014 and the FDA has classified it as Class I.
Check your package
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-2332-2014
- FDA event ID
- 68880
- Recalling firm
- BrandStorm, Van Nuys, CA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Jul 2014
- FDA classified
- 18 Aug 2014
- Reported
- 27 Aug 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Salmonella
- Product category
- Fish
Timeline
| 21 Jul 2014 | Recall initiated by company | |
| 18 Aug 2014 | Classified by FDA | +28 days |
| 27 Aug 2014 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
BrandStorm is recalling Organic Carob Powder because it may be contaminated with Salmonella.
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
Organic Carob Powder, Net Wt. 55lbs (25kg), Product Code: CAROB-100
Where it was distributed
North Dakota
Questions about this recall
Is Organic Carob Powder recalled?
Yes. BrandStorm recalled Organic Carob Powder on 21 Jul 2014. The recall is Class I and its status is Terminated. Recall number F-2332-2014.
Why was it recalled?
BrandStorm is recalling Organic Carob Powder because it may be contaminated with Salmonella.
Which lots are affected?
Lot Code: AN-395-13
Where was it sold?
North Dakota
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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