Check the Batch
Class ITerminated in FDA datasetRecall initiated Sep 23, 2019

Carolyn's Cookie Company - Frozen Cookie Doughballs - Bake at Home. Oatmeal Chocolate Chip Net…

Recalling firm: California New foods

Why it was recalled

Firm received consumer complaint of an allergic reaction after consumption.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 8, 2020.

Check your package

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

ProductCarolyn's Cookie Company - Frozen Cookie Doughballs - Bake at Home. Oatmeal Chocolate Chip Net Wt. 22 oz. (623.7g) UPC Code 680569160300
Package size22 oz
UPC680569160300

FDA code information

All date codes beginning April 7, 2019 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220

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

Full FDA record and distribution details

Original product description

Carolyn's Cookie Company - Frozen Cookie Doughballs - Bake at Home. Oatmeal Chocolate Chip Net Wt. 22 oz. (623.7g) UPC Code 680569160300

Extracted codes and context

TypeCode / valueContext
UPC680569160300lls - Bake at Home. Oatmeal Chocolate Chip Net Wt. 22 oz. (623.7g) UPC Code 680569160300
lot102519020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot10719h 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot111519ot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot121619: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot12420 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot162042719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot22220 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot31220 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot42719l date codes beginning April 7, 2019 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot4719All date codes beginning April 7, 2019 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot51519codes beginning April 7, 2019 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot52519eginning April 7, 2019 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot61919g April 7, 2019 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot71019 7, 2019 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot731199 through March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220
lot91119gh March 29, 2020 Lot Codes: 4719, 42719, 51519, 52519, 61919, 71019, 73119, 91119, 10719, 102519, 111519, 121619, 1620, 12420, 22220, 31220

Original FDA recall reason

Firm received consumer complaint of an allergic reaction after consumption.

Recall details

Recall number
F-0143-2020
Event ID
83866
FDA status
Terminated
Initiated
Sep 23, 2019
Reported
Nov 20, 2019
Classified
Nov 8, 2019
Terminated
Jan 8, 2020
Quantity
8,923 cases total
Location
Castroville, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

U.S. distribution to CA and NV. No foreign distribution.

FDA source record · F-0143-2020

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

Follow official FDA and manufacturer guidance.