Premo Asiago Italian Item # 207919, Net Wt 6 oz; Fresh Grab Asiago Italian Item # 251847, Net Wt 6 oz; Core-Mark Asiago Italian Item # 568377, Net Wt 6 oz;

Class I - Dangerous
Recalled: February 21, 2017 Lipari Foods Other Foods

What Should You Do?

  1. Check if you have this product:
    Item #: 207919, Lot #s: 05201701, 06201701, 09201701, 10201701, 11201701, 13201701, 16201701, 18201701, Best By 1/26/17 to 2/8/17; Item # 251847, Lot #s: 025201701, 06201701, 10201701, 17201701, Best By: 1/26/17 to 2/7/17; Item # 568377, Lot #s: 06201701 and 13201701, Best By: 1/26/17 and 1/27/17
  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:
Lipari Foods, Inc.
Reason for Recall:
JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to 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:

Premo Asiago Italian Item # 207919, Net Wt 6 oz; Fresh Grab Asiago Italian Item # 251847, Net Wt 6 oz; Core-Mark Asiago Italian Item # 568377, Net Wt 6 oz;

Product Codes/Lot Numbers:

Item #: 207919, Lot #s: 05201701, 06201701, 09201701, 10201701, 11201701, 13201701, 16201701, 18201701, Best By 1/26/17 to 2/8/17; Item # 251847, Lot #s: 025201701, 06201701, 10201701, 17201701, Best By: 1/26/17 to 2/7/17; Item # 568377, Lot #s: 06201701 and 13201701, Best By: 1/26/17 and 1/27/17

Distribution:

Distributed in: MI, IL, IN, KY, MD, OH, PA, TN, VA, WI, WV

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1829-2017

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