CLASS II Food recall · Reported 11 Nov 2015 · FDA Enforcement Report

Kontos Falafel Mix recalled

Kontos Foods is recalling Kontos Falafel Mix, distributed nationwide in the US. The recall was initiated on 1 Oct 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lot codes
Quantity recalled3,392 tubs

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-148-2016
FDA event ID
72342
Recalling firm
Kontos Foods, Paterson, NJ
Classification
Class II
Status
Terminated
Recall initiated
1 Oct 2015
FDA classified
4 Nov 2015
Reported
11 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
FAX
Product category
Other

Timeline

1 Oct 2015Recall initiated by company
4 Nov 2015Classified by FDA+34 days
11 Nov 2015Published 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

Kontos Falafel Mix contains undeclared wheat allergen.

Product as listed by the FDA

Kontos Falafel Mix Net Wt. 5 LBS. (2.27kg) Distributed by Kontos Foods Inc., Paterson, New Jersey 07544 UPC 0-32394-7027-7 #70271

Where it was distributed

nationwide

Nationwide

Questions about this recall

Is Kontos Falafel Mix recalled?

Yes. Kontos Foods recalled Kontos Falafel Mix on 1 Oct 2015. The recall is Class II and its status is Terminated. Recall number F-148-2016.

Why was it recalled?

Kontos Falafel Mix contains undeclared wheat allergen.

Which lots are affected?

All lot codes

Where was it sold?

nationwide

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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