Udderly Chocolate ice cream (item #67045), packaged in 1.75 qt. container. UPC 0 72830 07045 4. The label is read in parts: "***Tillamook*** ICE CREAM*** UDDERLY CHOCOLATE *** CONTAINS: MILK, TREE NUTS (COCONUT), SOY, EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES PRODUCTS CONTAINING PEANUTS, AND WHEAT.***"
Class I - DangerousWhat Should You Do?
- Check if you have this product: 41-80 092019 BEST IF USED BY AUG 28 19 06-26 8240 HH:MM BEST IF USED BY OCT 03 19 06-26 8276 HH:MM
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- Udderly Chocolate ice cream (item #67045), packaged in 1.75 qt. container, 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:
Udderly Chocolate ice cream (item #67045), packaged in 1.75 qt. container. UPC 0 72830 07045 4. The label is read in parts: "***Tillamook*** ICE CREAM*** UDDERLY CHOCOLATE *** CONTAINS: MILK, TREE NUTS (COCONUT), SOY, EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES PRODUCTS CONTAINING PEANUTS, AND WHEAT.***"
Product Codes/Lot Numbers:
41-80 092019 BEST IF USED BY AUG 28 19 06-26 8240 HH:MM BEST IF USED BY OCT 03 19 06-26 8276 HH:MM
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.govFDA Recall Number: F-0695-2019
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