Natural Delight Collection Natural Dried Apricots, product of Uzbekistan; in a 500 g (17 oz) cardboard box marked with
Summary
The FDA issued a Class I for Natural Delight Collection Natural Dried Apricots, product of Uzbekistan; in a by ILG International Trading, Inc.. Reason: Product contains undeclared sulfites..
Details
Source
Food Recall
External ID
F-0220-2022
Action Date
2021-12-08
Status
Terminated
Category
food
Product Description
Natural Delight Collection Natural Dried Apricots, product of Uzbekistan; in a 500 g (17 oz) cardboard box marked with a best before date of 03/30/2022. The product UPC code is 811579000533
Lot/Code Info: best before date of 03/30/2022. The product UPC code is 811579000533
Quantity Affected: 374
Reason for Recall
Product contains undeclared sulfites.
Distribution
NY, NJ, CA
Type: Voluntary: Firm initiated
Recall Initiated: 2021-11-05
Company
Brooklyn, NY
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 48 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 (ILG International Trading, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ILG International Trading, Inc. have FDA actions?
This is the only FDA action we have on record for ILG International Trading, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0220-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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