🔍 RecallPedia

SE Grocers Cheesecake SAMPLER New York Style, Chocolate Silk, Strawberry Swirl, Turtle - NO ARTIFICIAL FLAVORS - NET WT 32 OZ (2 LB) 907g - UPC 0 38259 13495 5 CONTAINS: EGG, MILK, SOY, AND WHEAT. MANUFACTURED IN A FACILITY THAT ALSO PROCESSES PEANUTS, TREE NUTS (ALMONDS, COCONUT, PECANS, WALNUTS) DISTRIBUTED BY: SOUTHEASTERN GROCERS, 8928 PROMINENCE PKWY, BLDG 200, JACKSONVILLE, FL 32256

Class I - Dangerous
Recalled: April 26, 2022 Atlanta Cheesecake Company Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Lot code 22091A2, Expiration Date 12/29/2022
  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:
Atlanta Cheesecake Company LLC
Reason for Recall:
The firm was notified by a customer that the label does not declare pecans in its ingredient statement.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

SE Grocers Cheesecake SAMPLER New York Style, Chocolate Silk, Strawberry Swirl, Turtle - NO ARTIFICIAL FLAVORS - NET WT 32 OZ (2 LB) 907g - UPC 0 38259 13495 5 CONTAINS: EGG, MILK, SOY, AND WHEAT. MANUFACTURED IN A FACILITY THAT ALSO PROCESSES PEANUTS, TREE NUTS (ALMONDS, COCONUT, PECANS, WALNUTS) DISTRIBUTED BY: SOUTHEASTERN GROCERS, 8928 PROMINENCE PKWY, BLDG 200, JACKSONVILLE, FL 32256

Product Codes/Lot Numbers:

Lot code 22091A2, Expiration Date 12/29/2022

Distribution:

Distributed in: FL, LA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1073-2022

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