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Gilster-Mary Lee Corp. Recall: Butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes and therefore contain undeclared milk

United States

TerminatedClass I

Company
Gilster-Mary Lee Corp.
Product
Organic Microwave Butter Popcorn in cartons labeled to be Or…
Recall date
May 25, 2021
Terminated
July 19, 2021
Source
FDA

Reason for recall

Butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes and therefore contain undeclared milk

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Organic Microwave Butter Popcorn in cartons labeled to be Organic Microwave Popcorn Salted, Net Wt 8.7 OZ, Distributed by TOPCO Associates LLC Elk Grove, IL, UPC 0 36800 40611 7 Not published in this source record 413 cases Best By APR 09 22, Lot APR0922N2

Distribution

  • Distributed to distribution centers in AZ
  • CA
  • CT
  • MI
  • MN
  • NH
  • NY
  • PA and UT

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0659-2021
Event ID
87997
Status
Terminated
Classification
Class I
Company
Gilster-Mary Lee Corp.
Product description
Organic Microwave Butter Popcorn in cartons labeled to be Organic Microwave Popcorn Salted, Net Wt 8.7 OZ, Distributed by TOPCO Associates LLC Elk Grove, IL, UPC 0 36800 40611 7
Quantity
413 cases
Reason
Butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes and therefore contain undeclared milk
Recall initiation date
May 25, 2021
Report date
June 16, 2021
Classification date
Not published in this source record
Termination date
July 19, 2021
Distribution pattern
Distributed to distribution centers in AZ, CA, CT, MI, MN, NH, NY, PA and UT
UPC, lot, and code information
Best By APR 09 22, Lot APR0922N2
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Gilster-Mary Lee Corp.

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FDA Recall United States Terminated Historical recordClass II

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Product
Cadia Organic Unsalted Microwave Popcorn, Net Wt. 8.4 oz (2…
Published
September 30, 2020
Distribution
Distributed to grocery stores in the fol…

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FDA Recall United States Terminated Historical recordClass II

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Product
Microwave popcorn packaged in the following ways: 1) Full…
Published
September 30, 2020
Distribution
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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Arizona 1
California 1
Connecticut 1
Michigan 1
Minnesota 1
New Hampshire 1
New York 1
Pennsylvania 1
Utah 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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?

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