🔍 RecallPedia

FINLANDIA SRIRACHA JACK & JALAPENO JACK CHEESE NET WT. 12 OZ. (340g) SRIRACHA JACK INGREDIENTS: PASTEURIZED MILK, CULTURES, SALT, JALAPENOS, CAYENNE GARLIC, CITRUS POWDER, ENZYMES CONTAINS: MILK JALAPENO JACK INGREDIENTS: PASTEURIZED MILK, RED AND GREEN JALAPENO PEPPERS, CULTURES, SALT, ENZYMES, ANNOTTO CONTAINS: MILK, DISTRIBUTED BY FINLANDIA CHEESE INC., PARSIPPANY, NJ 07054 UPC 6 73803 04508 2

Class I - Dangerous
Recalled: February 15, 2017 Biery Cheese Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Sell By JUL/19/17
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Biery Cheese, Inc.
Reason for Recall:
The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

FINLANDIA SRIRACHA JACK & JALAPENO JACK CHEESE NET WT. 12 OZ. (340g) SRIRACHA JACK INGREDIENTS: PASTEURIZED MILK, CULTURES, SALT, JALAPENOS, CAYENNE GARLIC, CITRUS POWDER, ENZYMES CONTAINS: MILK JALAPENO JACK INGREDIENTS: PASTEURIZED MILK, RED AND GREEN JALAPENO PEPPERS, CULTURES, SALT, ENZYMES, ANNOTTO CONTAINS: MILK, DISTRIBUTED BY FINLANDIA CHEESE INC., PARSIPPANY, NJ 07054 UPC 6 73803 04508 2

Product Codes/Lot Numbers:

Sell By JUL/19/17

Distribution:

Distributed in: FL, GA, IL, IN, KY, MA, MI, NJ, OH, PA, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1842-2017

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