ARASHAN brand mixed dried fruit packaged in 1lb clear plastic bags with a sticker label. UPC: 850008491368
Summary
The FDA issued a Class II for ARASHAN brand mixed dried fruit packaged in 1lb clear plastic bags with a sticke by Bek12 Inc. Reason: Undeclared sulfites.
Details
Source
Food Recall
External ID
F-0192-2023
Action Date
2022-12-14
Status
Terminated
Category
food
Product Description
ARASHAN brand mixed dried fruit packaged in 1lb clear plastic bags with a sticker label. UPC: 850008491368
Lot/Code Info: "Production date: 02.23.2022 Best before: 02.23.2022" and "Production date: 04.2022 Best before 12.2024"
Quantity Affected: 4,186 units
Reason for Recall
Undeclared sulfites
Distribution
Product is distributed to Illinois, New York, New Jersey, and Pennsylvania
Type: Voluntary: Firm initiated
Recall Initiated: 2022-11-07
Company
Arlington Heights, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 16 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Bek12 Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bek12 Inc have FDA actions?
This is the only FDA action we have on record for Bek12 Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0192-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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