EGG CUSTARD PIE, NET WT 25 OZ (1 LB 9 OZ) 709 g, packaged in paper carton with plastic film window, 6 cartons per case.

Class I - Dangerous
Recalled: November 16, 2023 Publix Super Markets Other Foods

What Should You Do?

  1. Check if you have this product:
    Coconut Custard Pie master case (shipped frozen) was labeled with expiration date of Feb-26-2024, Lot #: 101923B1. Individual pie cartons were labeled with a 3-day shelf life at the retail stores when placed on refrigerated display for sale (thawed). Dates on individual pie cartons offered for sale to customers may range from sell by date of 10/22/23 through sell by date of 11/18/23.
  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:
Publix Super Markets, Inc.
Reason for Recall:
Undeclared Tree Nut (Coconut)
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

EGG CUSTARD PIE, NET WT 25 OZ (1 LB 9 OZ) 709 g, packaged in paper carton with plastic film window, 6 cartons per case.

Product Codes/Lot Numbers:

Coconut Custard Pie master case (shipped frozen) was labeled with expiration date of Feb-26-2024, Lot #: 101923B1. Individual pie cartons were labeled with a 3-day shelf life at the retail stores when placed on refrigerated display for sale (thawed). Dates on individual pie cartons offered for sale to customers may range from sell by date of 10/22/23 through sell by date of 11/18/23.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0655-2024

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