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FDA source record Class II Terminated

Karison brand PANJIRI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Almonds, Sugar, Lotus Seeds, Fennel Seeds, Flax Seeds, Edible Gum, Ginger Powder, Zero Trans Fat Vegetab...

Recall Date: 2026-01-06 Recalling Firm: Karison Foods & Snacks, Inc. Record Ref: H-0509-2026

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns Karison brand PANJIRI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Almonds, Sugar, Lotus Seeds, Fennel Seeds, Flax Seeds, Edible Gum, Ginger Powder, Zero Trans Fat Vegetab... and names Karison Foods & Snacks, Inc. 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: Karison Foods & Snacks, Inc.
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2026-01-06
Best identifiers to check for a FDA record

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Product Description & Identification

Karison brand PANJIRI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Almonds, Sugar, Lotus Seeds, Fennel Seeds, Flax Seeds, Edible Gum, Ginger Powder, Zero Trans Fat Vegetable Shortening; UPC: 8 97307 00243 7; Distributed By: Karison Foods & Snacks Inc.; 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.

Reason for Recall / Hazard Identified

Product contains milk, which is undeclared in the ingredient statement.

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

NY, NJ, VA

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:12 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
H-0509-2026
Indexed update
2026-08-09 21:59:12 UTC
Official source
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