Linden's brand Chocolate Chip Cookies: a) Chocolate Chippers Bite Size Cookies (Mini), NET WT. 2 OZ., UPC 76809-30017; b) Chocolate Chippers (Mini), NET WT 1.1 OZ., UPC 76809-30090; c) 3 LARGE CHOCOLATE CHIP COOKIES (Pack), NET WT. 1.75 OZ. UPC 76809-30010 --- LINDEN COOKIES, INC. 25 BRENNER DRIVE CONGERS, NY 10920

Class I - Dangerous
Recalled: December 13, 2016 Linden Cookies Bakery & Bread

What Should You Do?

  1. Check if you have this product:
    a): Sell By Dates Feb. 8, 2017 through March 28, 2017; b): Sell By Dates Feb. 8, 2017 through March 28, 2017; c): Dec. 14, 2016 through Feb 01, 2017
  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:
Linden Cookies, Inc
Reason for Recall:
The product contains undeclared milk from the bulk chocolate chips received from the supplier.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Linden's brand Chocolate Chip Cookies: a) Chocolate Chippers Bite Size Cookies (Mini), NET WT. 2 OZ., UPC 76809-30017; b) Chocolate Chippers (Mini), NET WT 1.1 OZ., UPC 76809-30090; c) 3 LARGE CHOCOLATE CHIP COOKIES (Pack), NET WT. 1.75 OZ. UPC 76809-30010 --- LINDEN COOKIES, INC. 25 BRENNER DRIVE CONGERS, NY 10920

Product Codes/Lot Numbers:

a): Sell By Dates Feb. 8, 2017 through March 28, 2017; b): Sell By Dates Feb. 8, 2017 through March 28, 2017; c): Dec. 14, 2016 through Feb 01, 2017

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1222-2017

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