Ground Elk meat packaged individually for retail sale in hermetically sealed plastic with a black backing identified with Use or Freeze By 04-27-15. The stick-on finished product label is red, white, and black with red, white, and black print writing reading in part: "Natural DK Meats All Natural Ground Elk Net Wt 16 oz Packed for DK Natural Meats Asheville, NC 28806, UPC 055173061006".
Class I - DangerousWhat Should You Do?
- Check if you have this product: Use or Freeze by date of 04-27-15, product code number 80018, UPC 055173061006.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- Frontiere Natural Meats
- Reason for Recall:
- Frontiere Natural Meats, LLC of Denver, Colorado is recalling certain 16 ounce packages of ground elk meat due to potential contamination with Escherichia coli O157:H7.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Ground Elk meat packaged individually for retail sale in hermetically sealed plastic with a black backing identified with Use or Freeze By 04-27-15. The stick-on finished product label is red, white, and black with red, white, and black print writing reading in part: "Natural DK Meats All Natural Ground Elk Net Wt 16 oz Packed for DK Natural Meats Asheville, NC 28806, UPC 055173061006".
Product Codes/Lot Numbers:
Use or Freeze by date of 04-27-15, product code number 80018, UPC 055173061006.
Distribution:
Distributed in: NC
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-2783-2015
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