Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Packs Net Wt 3 lbs Mondelez International Mondelez Global LLC East Hanover, NJ 07936 USA Made in Mexico case UPC 0 44000 03445 0 Inner Pouch: Nabisco Newtons Fig Net Wt 2 oz (56 g) Mondelez Global LLC, East Hanover, NJ 07936 Made in Mexico retail UPC 0 44000 03445 0

Class I - Dangerous
Recalled: May 13, 2015 Mondelez International Other Foods Nationwide

What Should You Do?

  1. Check if you have this product:
    07 SEP 2015 09 OCT 2015 10 OCT 2015 25 OCT 2015 26 OCT 2015 17 NOV 2015 18 NOV 2015 27 NOV 2015 29 NOV 2015 30 NOV 2015
  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:
Mondelez International
Reason for Recall:
Fig Newtons brand Club Super Carton cookie products is mislabeled. The outer carton does not declare milk but the inner carton does.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Packs Net Wt 3 lbs Mondelez International Mondelez Global LLC East Hanover, NJ 07936 USA Made in Mexico case UPC 0 44000 03445 0 Inner Pouch: Nabisco Newtons Fig Net Wt 2 oz (56 g) Mondelez Global LLC, East Hanover, NJ 07936 Made in Mexico retail UPC 0 44000 03445 0

Product Codes/Lot Numbers:

07 SEP 2015 09 OCT 2015 10 OCT 2015 25 OCT 2015 26 OCT 2015 17 NOV 2015 18 NOV 2015 27 NOV 2015 29 NOV 2015 30 NOV 2015

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2932-215

Related Recalls