Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356, 1
Summary
The FDA issued a Class I for Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 07270 by Kenover Marketing Corp.. Reason: Undeclared milk due to mispackaging.
Details
Source
Food Recall
External ID
F-0608-2024
Action Date
2023-12-27
Status
Terminated
Category
food
Product Description
Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356, 12 bags per case. Product packaged in gold foil in blue netting bags.
Lot/Code Info: Lot 2283
Quantity Affected: 24 cases
Reason for Recall
Undeclared milk due to mispackaging
Distribution
Distributed to distributors and retailers in IL, PA, MD, CA, NH, RI, CO, OR, IA, FL, GA, TX, NY, NJ, SC, MA, WI and CT.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-01
Company
Bayonne, NJ
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 157 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kenover Marketing Corp. has 4 FDA actions in our database, including 4 recalls.
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 (Kenover Marketing Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kenover Marketing Corp. have FDA actions?
Kenover Marketing Corp. 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-0608-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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