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Craftmark Bakery, LLC Recall: Undeclared tree nut allergen.

United States

TerminatedClass II

Company
Craftmark Bakery, LLC
Product
Chocolate Chip Cookie Dough packaged in 1 case, 6 bags/case,…
Recall date
September 30, 2021
Terminated
February 15, 2022
Source
FDA

Reason for recall

Undeclared tree nut allergen.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Chocolate Chip Cookie Dough packaged in 1 case, 6 bags/case, and 30 frozen pies of dough/bag. Labeling reads "Chocolate Chip Cookie Dough***Tiff's Treats***Do not consume raw***" Not published in this source record 4,632 cases, 6 bags/case, 30 pieces of dough per bag. Lot 1: 1A232 Best by: 8/20/2022 Lot 2: 1B232 Best by: 8/20/2022

Distribution

  • 3 distributors and 68 retailers

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0133-2022
Event ID
88816
Status
Terminated
Classification
Class II
Company
Craftmark Bakery, LLC
Product description
Chocolate Chip Cookie Dough packaged in 1 case, 6 bags/case, and 30 frozen pies of dough/bag. Labeling reads "Chocolate Chip Cookie Dough***Tiff's Treats***Do not consume raw***"
Quantity
4,632 cases, 6 bags/case, 30 pieces of dough per bag.
Reason
Undeclared tree nut allergen.
Recall initiation date
September 30, 2021
Report date
November 10, 2021
Classification date
Not published in this source record
Termination date
February 15, 2022
Distribution pattern
3 distributors and 68 retailers
UPC, lot, and code information
Lot 1: 1A232 Best by: 8/20/2022 Lot 2: 1B232 Best by: 8/20/2022
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Telephone
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Craftmark Bakery, LLC

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Distribution
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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.