Food recall: Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356…
Class I FDA enforcement event 93518. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Undeclared milk due to mispackaging
Class I, in the words of FDA
a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death
Kenover Marketing Corp. started this food recall on 1 Dec 2023. The firm address in the FDA record is in Bayonne, NJ. FDA put the recall in Class I. FDA event 93518 has 1 product record. The first FDA enforcement report date is 27 Dec 2023. The record gives the status Terminated, with the termination date 8 Oct 2024.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
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.
Recalling firm
Kenover Marketing Corp., Bayonne, NJ.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
1 product record in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0608-2024 | 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. | 24 cases | Class I | Terminated | 27 Dec 2023 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class I: The highest of the three FDA recall classes.
The event in context
- Food events that started in 2023
- 478
- Share of these events in Class I
- 35%
- Product records in this event
- 1Median of the firm: 1
- Events of the firm on the register
- 4
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 17 Feb 2025 | Glicks Dark Chocolate Conettos, 2.47 oz., Plastic Bag, 24 packages per case | Food | Class I | 1 |
| 3 May 2023 | Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) bottle, UPC 858313006208, 8 Units per case. | Food | Class I | 1 |
| 23 Aug 2022 | "Mighty Sesame 10.9oz Organic Tahini" in a 10.9oz plastic squeeze bottle, 8 Units per Cases . | Food | Class I | 1 |
Official channels
- FDA enforcement report F-0608-2024The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 93518. https://recallregister.com/fda/i/93518/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this 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.
- What quantity of product is in FDA event 93518?
- The FDA record gives this quantity:
24 cases
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2023 have the same class?
- 35% of the 478 food events that started in 2023 are in Class I.