CLASS I Food recall · Reported 12 Jan 2022 · FDA Enforcement Report

Godavari Apricots recalled by Bokhary Foods

Bokhary Foods is recalling Godavari Apricots, distributed in Connecticut, Massachusetts, New York. The recall was initiated on 10 Dec 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes7-oz product 14-oz product There is no other coding on the packaging.
Quantity recalled3-28lb boxes

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-0362-2022
FDA event ID
89207
Recalling firm
Bokhary Foods, Lawrence, MA
Classification
Class I
Status
Terminated
Recall initiated
10 Dec 2021
FDA classified
5 Jan 2022
Reported
12 Jan 2022
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
Peaches

Timeline

10 Dec 2021Recall initiated by company
5 Jan 2022Classified by FDA+26 days
12 Jan 2022Published 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

Products contain undeclared sulfites.

Product as listed by the FDA

GODAVARI brand APRICOTS, packaged in 7 oz (UPC 0 03658 50001 4) and 14 oz (UPC 0 03657 5001 5) clear plastic-film bags with the GODAVARI brand label on the front. Each bag is filled with orange-colored dried apricots that can be seen through the bag.

Where it was distributed

MA, CT, NY

ConnecticutMassachusettsNew York

Questions about this recall

Why was it recalled?

Products contain undeclared sulfites.

Which lots are affected?

7-oz product 14-oz product There is no other coding on the packaging.

Where was it sold?

MA, CT, NY

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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