🔍 RecallPedia

1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton

Class I - Dangerous
🍎 Food Recalled: May 24, 2022 Calico Cottage Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    1. GTIN: 00673305110936 LOT: 22069041, 22104149, 22118292 2. GTIN: 00673305039084 LOT: 22103099, 22130389 3. GTIN: 00673305039091 LOT: 22074033, 22089039, 22101075, 22103102, 22111217, 22136439, 22137455, 22139488
  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:
Calico Cottage Inc
Reason for Recall:
Fudge contains peanut butter that is potentially contaminated with Salmonella.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton

Product Codes/Lot Numbers:

1. GTIN: 00673305110936 LOT: 22069041, 22104149, 22118292 2. GTIN: 00673305039084 LOT: 22103099, 22130389 3. GTIN: 00673305039091 LOT: 22074033, 22089039, 22101075, 22103102, 22111217, 22136439, 22137455, 22139488

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1337-2022

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