🔍 RecallPedia

Tillamook Mudslide ice cream (item #63006), packaged in 3 gallon tub. UPC 0 72830 63006 1. The label is read in parts: "***TILLAMOOK MUDSLIDE ICE CREAM*** ALLERGEN INFORMATION: This product contains milk, peanut, soy, tree nut (coconut), egg. It is made with equipment that also makes product containing wheat.***"

Class I - Dangerous
Recalled: November 16, 2018 TILLAMOOK COUNTY CREAMERY ASSOC Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Best Buy Date 4/16/20 HH:MM:SS 41-80
  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:
TILLAMOOK COUNTY CREAMERY ASSOC
Reason for Recall:
Tillamook Mudslide ice cream (item #63006), packaged in 3-gallon tub, is recalled because product contains trace amounts of undeclared color additives Amaranth and Yellow No. 6 in the chocolate freckles and chocolate fudge pieces ingredients.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Tillamook Mudslide ice cream (item #63006), packaged in 3 gallon tub. UPC 0 72830 63006 1. The label is read in parts: "***TILLAMOOK MUDSLIDE ICE CREAM*** ALLERGEN INFORMATION: This product contains milk, peanut, soy, tree nut (coconut), egg. It is made with equipment that also makes product containing wheat.***"

Product Codes/Lot Numbers:

Best Buy Date 4/16/20 HH:MM:SS 41-80

Distribution:

Distributed in: AZ, CA, CO, GA, ID, MN, NV, OR, TX, UT, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0692-2019

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