CLASS I Food recall · Reported 19 Dec 2012 · FDA Enforcement Report

Turkana Valley Dried Apricot recalled

Turkana Food is recalling Turkana Valley Dried Apricot. The recall was initiated on 15 Nov 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes250 g- Best Before 02/2013 Lot #11-4 500 g- Best Before 02/2013 Lot #11-3
Quantity recalled147 boxes (250g each); 194 boxes (500g each)

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-0807-2013
FDA event ID
63693
Recalling firm
Turkana Food, Kenilworth, NJ
Classification
Class I
Status
Terminated
Recall initiated
15 Nov 2012
FDA classified
12 Dec 2012
Reported
19 Dec 2012
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Turkey

Timeline

15 Nov 2012Recall initiated by company
12 Dec 2012Classified by FDA+27 days
19 Dec 2012Published in enforcement report+7 days

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

Reason for recall

Turkana Valley dried apricots contain undeclared sulfites which was discovered during NYSDAM sampling.

Product as listed by the FDA

Turkana Valley Dried Apricot 250 g, UPC 8692594007804 and 500 g UPC 8692594007811 Tunas Gida, San Ve Tic. Ltd. Sti 2 Org. San. Bol. Celal Dogan Bulvari No.:3 Baspinar Gaziantep/ Turkey packaged in plastic container

Where it was distributed

Northeast

Questions about this recall

Why was it recalled?

Turkana Valley dried apricots contain undeclared sulfites which was discovered during NYSDAM sampling.

Which lots are affected?

250 g- Best Before 02/2013 Lot #11-4 500 g- Best Before 02/2013 Lot #11-3

Where was it sold?

Northeast

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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