Giant Eagle Breaded Shrimp Pittsburgh, PA 15238 PLU # 86815 refrigerated, packed in plastic clam shell. Sell by dates: up to and including Oct 25 2017. Located in the Grab "n Go refrigerated cases at Giant Eagle and Market District supermarkets.

Class I - Dangerous
Recalled: October 19, 2017 Giant Eagle Seafood

What Should You Do?

  1. Check if you have this product:
    up to and including Sell By: Oct 25 17. PLU # 86815
  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:
Giant Eagle Voluntarily Recalls Breaded Shrimp Due to an Undeclared Egg Allergen. All lot codes up to and including best by October 24, 2017 of Giant Eagle brand Breaded Shrimp, prepared and sold from the Prepared Foods grab and go sections inside Giant Eagle and Market District supermarkets through October 19, 2017 have been voluntarily recalled by Giant Eagle due to an undeclared egg allergen.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Giant Eagle Breaded Shrimp Pittsburgh, PA 15238 PLU # 86815 refrigerated, packed in plastic clam shell. Sell by dates: up to and including Oct 25 2017. Located in the Grab "n Go refrigerated cases at Giant Eagle and Market District supermarkets.

Product Codes/Lot Numbers:

up to and including Sell By: Oct 25 17. PLU # 86815

Distribution:

Distributed in: MD, OH, PA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0334-2018

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