RECALL RECORD — CLASS IIRecall closedF-0694-2019/FDA enforcement

Vanilla Chocolate Chip Ice Cream (Item #67017), Packaged in 1.75 Qt

What you need to know

Class II
  • What happened

    Vanilla Chocolate Chip ice cream (item #67017), packaged in 1.75 qt. container, is recalled because product contains trace amounts of undeclared color additives Amaranth and…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Tree nuts such as almonds or walnuts were not declared, posing a risk to people with tree-nut allergy.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAIN, AZ, CA, CO +8 moreMore food

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Product identification

Source: FDA FOOD

Brand nameTillamook County Creamery Assoc
Recalling firmTillamook County Creamery AssocTillamook, OR, United States
UPC / barcodes
0 72830 07017 12 51906 26817 61 31906 26825 61 81906 26829 1
Lot / date codes
  • -BEST IF USED BY JUN 25 19 06-26 8176 HH:MM -BEST IF USED BY 10/18/2019 PLANT 04-116 (3) 000000 HH:MM -41-80 BB 082719 -BEST IF USED BY SEP 13 19 06-26 8256 HH:MM -BEST IF USED BY OCT 18 19 06-26 8291 HH:MM
Distribution area
INAZCACOGAIDMNNVORTXUTWA

distributed in AZ, CA, CO, GA, ID, MN, NV, OR, TX, UT, and WA.

United States

Quantity affected11, 306 cases (6/1.75 qt. containers per case)
Recall initiationFDA report date: December 12, 2018
FDA recall numberF-0694-2019

Beyond the headline

The recall, in context

Tillamook County Creamery Assoc initiated this food recall on November 16, 2018. The FDA enforcement report states: Vanilla Chocolate Chip ice cream (item #67017), 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. The FDA report lists distribution as: distributed in AZ, CA, CO, GA, ID, MN, NV, OR, TX, UT, and WA.

The FDA enforcement report describes the reason as: Vanilla Chocolate Chip ice cream (item #67017), 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.

Vanilla Chocolate Chip Ice Cream (Item #67017), Packaged in 1.75 Qt was made or distributed by Tillamook County Creamery Assoc in Tillamook, OR, United States. This page reflects FDA report F-0694-2019, dated December 12, 2018.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared tree nuts

Symptoms to watch for

Hives, swelling, wheezing, digestive symptoms or anaphylaxis can occur in people with a tree-nut allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed tree-nut allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a tree-nut allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Vanilla Chocolate Chip Ice Cream (Item #67017), Packaged in 1.75 Qt recall?

Tillamook County Creamery Assoc recalled Vanilla Chocolate Chip Ice Cream (Item #67017), Packaged in 1.75 Qt in an FDA Class II enforcement action reported as F-0694-2019. Vanilla Chocolate Chip ice cream (item #67017), packaged in 1.75 qt. container, is recalled because product contains trace amounts of undeclared color additives Amaranth and…

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a tree-nut allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Tillamook County Creamery Assoc recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0694-2019. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Tillamook County Creamery Assoc

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.