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FDA source record Class I Terminated

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 ne...

Recall Date: 2023-12-01 Recalling Firm: Kenover Marketing Corp. Record Ref: F-0608-2024

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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 ne... and names Kenover Marketing Corp. as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: Kenover Marketing Corp.
  • Classification: Class I
  • Status: Terminated
  • Recall date: 2023-12-01
Best identifiers to check for a FDA record

Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.

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Product Description & Identification

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.

Reason for Recall / Hazard Identified

Undeclared milk due to mispackaging

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

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.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0608-2024
Indexed update
2026-08-09 21:59:13 UTC
Official source
Open issuing-agency record