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Jimmy's Cookies Recall: The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk. - F-2186-2017

United States

TerminatedClass I

Company
Jimmy's Cookies
Product
The Bakery Peanut Butter Chocolate Chunk Cookies, Net Wt. 14…
Recall date
April 11, 2017
Terminated
August 31, 2017
Source
FDA

Reason for recall

The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
The Bakery Peanut Butter Chocolate Chunk Cookies, Net Wt. 14 oz. (396g), packaged in a clear plastic clam shell, UPC 0 78742 06652 3, Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716 Not published in this source record 3,834 cases (12 packages per case) Lot #047

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2186-2017
Event ID
77027
Status
Terminated
Classification
Class I
Company
Jimmy's Cookies
Product description
The Bakery Peanut Butter Chocolate Chunk Cookies, Net Wt. 14 oz. (396g), packaged in a clear plastic clam shell, UPC 0 78742 06652 3, Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716
Quantity
3,834 cases (12 packages per case)
Reason
The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.
Recall initiation date
April 11, 2017
Report date
May 17, 2017
Classification date
Not published in this source record
Termination date
August 31, 2017
Distribution pattern
Nationwide
UPC, lot, and code information
Lot #047
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Jimmy's Cookies

Where this information comes from

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

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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 I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of August 31, 2017.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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.

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