Kenover Marketing Corp.
Kenover Marketing Corp. has 4 FDA enforcement events on this register (4 product records) between 2022 and 2025: 4 food; the busiest year was 2023 with 2.
100% of its events are Class I; the most common class is Class I (4). 0 events are listed as ongoing; the recalling firm's address is in NJ.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 17 Feb 2025 | Glicks Dark Chocolate Conettos, 2.47 oz., Plastic Bag, 24 packages per case | Food | Class I | 1 | Terminated |
| 1 Dec 2023 | 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. | Food | Class I | 1 | Terminated |
| 3 May 2023 | Mighty Sesame 10.9 Oz Organic Tahini (Squeezable) bottle, UPC 858313006208, 8 Units per case. | Food | Class I | 1 | Terminated |
| 23 Aug 2022 | "Mighty Sesame 10.9oz Organic Tahini" in a 10.9oz plastic squeeze bottle, 8 Units per Cases . | Food | Class I | 1 | Terminated |
By type and class
Class I: 100% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Kenover Marketing Corp. had?
4 enforcement events (4 product records) on this register, 2022–2025: 4 food.
Are any Kenover Marketing Corp. recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are Kenover Marketing Corp. recalls?
4 Class I. 100% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.