Sekeroglu Lokum Love Turkish Delight With Pistachio And Pomegranate Flavor Double Roasted Delight 350 grams UPC:86834540
Summary
The FDA issued a Class II for Sekeroglu Lokum Love Turkish Delight With Pistachio And Pomegranate Flavor Doubl by Turkana Food Inc.. Reason: Product contains Acid Red 18.
Details
Source
Food Recall
External ID
F-1119-2024
Action Date
2024-04-10
Status
Terminated
Category
food
Product Description
Sekeroglu Lokum Love Turkish Delight With Pistachio And Pomegranate Flavor Double Roasted Delight 350 grams UPC:8683454050542. Packaged in a paper carton. 25 cartons per case.
Lot/Code Info: Lot No: L 231023NCKL, Exp Date: 10/22/24
Quantity Affected: 72 cases
Reason for Recall
Product contains Acid Red 18
Distribution
Distributed to retail stores in CA, CT, WI, IN, NJ, OH, FL, MA, RI, TX, IL, GA, TN, MD, PA,NJ, NC, MI, MN, VA, and NY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-15
Company
Kenilworth, NJ
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 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Turkana Food Inc. has 4 FDA actions in our database, including 4 recalls.
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 (Turkana Food Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Turkana Food Inc. have FDA actions?
Turkana Food Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1119-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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