GODAVARI brand APRICOTS, packaged in 7 oz (UPC 0 03658 50001 4) and 14 oz (UPC 0 03657 5001 5) clear plastic-film bags w
Summary
The FDA issued a Class I for GODAVARI brand APRICOTS, packaged in 7 oz (UPC 0 03658 50001 4) and 14 oz (UPC 0 by Bokhary Foods, Inc.. Reason: Products contain undeclared sulfites..
Details
Source
Food Recall
External ID
F-0362-2022
Action Date
2022-01-12
Status
Terminated
Category
food
Product Description
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.
Lot/Code Info: 7-oz product 14-oz product There is no other coding on the packaging.
Quantity Affected: 3-28lb boxes
Reason for Recall
Products contain undeclared sulfites.
Distribution
MA, CT, NY
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-10
Company
Lawrence, MA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 11 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Bokhary Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bokhary Foods, Inc. have FDA actions?
This is the only FDA action we have on record for Bokhary Foods, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0362-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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