CLASS I Food recall · Reported 27 Aug 2014 · FDA Enforcement Report

Organic Carob Powder Light recalled by Ciranda

Ciranda is recalling Organic Carob Powder Light, distributed in California, Florida, Georgia, Iowa. The recall was initiated on 21 Jul 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 395-13
Quantity recalled359 bags ( 19,784.49 lbs)

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-2334-2014
FDA event ID
68859
Recalling firm
Ciranda, Hudson, WI
Classification
Class I
Status
Terminated
Recall initiated
21 Jul 2014
FDA classified
19 Aug 2014
Reported
27 Aug 2014
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Fish

Timeline

21 Jul 2014Recall initiated by company
19 Aug 2014Classified by FDA+29 days
27 Aug 2014Published in enforcement report+8 days

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

Reason for recall

Ciranda is recalling one lot of Organic Carob Powder Light after learning that a customer received a positive test for 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

Ciranda Organic Carob Powder Light, Product Code 20030. Net Wt. 55.11 lbs / 25 kg. Ingredients: Organic Carob Powder. Manufactured in Italy.

Where it was distributed

CA, FL, GA, and IA

CaliforniaFloridaGeorgiaIowa

Questions about this recall

Why was it recalled?

Ciranda is recalling one lot of Organic Carob Powder Light after learning that a customer received a positive test for Salmonella.

Which lots are affected?

Lot 395-13

Where was it sold?

CA, FL, GA, and IA

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.

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