CLASS III Food recall · Reported 21 Jun 2017 · FDA Enforcement Report

Aahu Barah, Dry Fig recalled by Global Commodities

Global Commodities is recalling Aahu Barah, Dry Fig, distributed in Massachusetts, New Jersey, New York, Virginia. The recall was initiated on 31 Mar 2017 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesBest Before: December 2019
Quantity recalled93 cases

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-2371-2017
FDA event ID
76897
Recalling firm
Global Commodities, Hicksville, NY
Classification
Class III
Status
Terminated
Recall initiated
31 Mar 2017
FDA classified
14 Jun 2017
Reported
21 Jun 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Sulfites
Product category
Other

Timeline

31 Mar 2017Recall initiated by company
14 Jun 2017Classified by FDA+75 days
21 Jun 2017Published 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

Presence of Undeclared Sulfites

Product as listed by the FDA

AAHU BARAH, DRY FIG, NET WT. 1 LB, PRODUCT OF PAKISTAN

Where it was distributed

NY, NJ, MA & VA

MassachusettsNew JerseyNew YorkVirginia

Questions about this recall

Is Aahu Barah, Dry Fig recalled?

Yes. Global Commodities recalled Aahu Barah, Dry Fig on 31 Mar 2017. The recall is Class III and its status is Terminated. Recall number F-2371-2017.

Why was it recalled?

Presence of Undeclared Sulfites

Which lots are affected?

Best Before: December 2019

Where was it sold?

NY, NJ, MA & VA

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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