🔍 RecallPedia

All varieties and packaging configurations of iced cut out cookies, labeled as Decorated Cut Out Cookie and Cut Out Cookies, 1oz and 2oz sold individually behind the bakery department service counter, and also pre-packaged in 2 counts (5oz), 10 counts (15oz), inside clear plastic containers, "processed on shared equipment" statement on label.

Class I - Dangerous
Recalled: March 17, 2015 Giant Eagle Bakery & Bread

What Should You Do?

  1. Check if you have this product:
    PLUs 17972 and 37973, all Sell By Dates through March 21st
  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:
Giant Eagle, Inc.
Reason for Recall:
Cut Out Cookies sold in Giant Eagle Bakeries were recalled due to an undeclared milk allergen detected after receiving a consumer complaint of an allergic reaction.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

All varieties and packaging configurations of iced cut out cookies, labeled as Decorated Cut Out Cookie and Cut Out Cookies, 1oz and 2oz sold individually behind the bakery department service counter, and also pre-packaged in 2 counts (5oz), 10 counts (15oz), inside clear plastic containers, "processed on shared equipment" statement on label.

Product Codes/Lot Numbers:

PLUs 17972 and 37973, all Sell By Dates through March 21st

Distribution:

Distributed in: PA, MD, OH, WV

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2043-2015

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