Class IITerminated in FDA datasetNov 16, 2018

Chocolaty Chip Cookie Dough ice cream (item #67016), packaged in 1.75 qt. container.

Recalling firm: TILLAMOOK COUNTY CREAMERY ASSOC

Why it was recalled

Chocolaty Chip Cookie Dough ice cream (item #67016), packaged in 1.75 qt. containers, 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.

Check your package

Compare the exact product and package details with the label you have.

ProductChocolaty Chip Cookie Dough ice cream (item #67016), packaged in 1.75 qt. container. UPC 0 72830 07016 4. The label is read in parts: "***Tillamook ***ICE CREAM *** CHOCOLATY CHIP COOKIE DOUGH *** CONTAINS: MILK, WHEAT, SOY, TREE NUTS (COCONUT), EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES PRODUCTS CONTAINING PEANUTS.***"
UPC072830070164

FDA code information

-BEST IF USED BY AUG 18 2019 -BEST IF USED BY SEP 25 2019 06-26 8268 HH:MM -BEST IF USED BY OCT 08 2019 06-26 8281 HH:MM -BEST IF USED BY OCT 24 2019 06-26 8297 HH:MM

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Chocolaty Chip Cookie Dough ice cream (item #67016), packaged in 1.75 qt. container. UPC 0 72830 07016 4. The label is read in parts: "***Tillamook ***ICE CREAM *** CHOCOLATY CHIP COOKIE DOUGH *** CONTAINS: MILK, WHEAT, SOY, TREE NUTS (COCONUT), EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES PRODUCTS CONTAINING PEANUTS.***"

Extracted codes and context

TypeCode / valueContext
UPC072830070164 Chip Cookie Dough ice cream (item #67016), packaged in 1.75 qt. container. UPC 0 72830 07016 4. The label is read in parts: "***Tillamook ***ICE CREAM *** CHOCOLATY CHIP COOKIE DOUGH *** CONTAINS: MILK, WHEAT, S
best byOCT 08 2019Y AUG 18 2019 -BEST IF USED BY SEP 25 2019 06-26 8268 HH:MM -BEST IF USED BY OCT 08 2019 06-26 8281 HH:MM -BEST IF USED BY OCT 24 2019 06-26 8297 HH:MM
best byOCT 24 201926 8268 HH:MM -BEST IF USED BY OCT 08 2019 06-26 8281 HH:MM -BEST IF USED BY OCT 24 2019 06-26 8297 HH:MM
best bySEP 25 2019-BEST IF USED BY AUG 18 2019 -BEST IF USED BY SEP 25 2019 06-26 8268 HH:MM -BEST IF USED BY OCT 08 2019 06-26 8281 HH:MM -BEST IF USED BY OCT 24 2019 06-26 8297 HH:MM

Recall details

Recall number
F-0693-2019
Event ID
81601
FDA status
Terminated
Initiated
Nov 16, 2018
Reported
Dec 12, 2018
Classified
Dec 6, 2018
Terminated
Apr 17, 2019
Quantity
5,362 cases (6/1.75 qt. containers per case)
Location
Tillamook, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

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

FDA source record · F-0693-2019

Data updated September 16, 2026. View official FDA data ↗

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