Gilster-Mary Lee Microwave Movie Theater Butter Popcorn Recall

Why it was recalled

Buttered popcorn contains a milk ingredient (butter), but fails to declare milk on the label.

Product description

Microwave Movie Theater Butter Popcorn, Naturally Flavored, Net Wt. 19.8 OZ (1 lb 3.8 OZ), Distributed by Schnuck Markets, Inc. St. Louis, MO 63146

Lot numbers, UPCs & expiration codes

OCT 12 19 G9

Where it was sold

To one customer distribution center in Missouri.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-0630-2019
Classification: Class II
Status: Terminated
Recall initiated: Oct 31, 2018
FDA report date: Nov 28, 2018
Quantity: 221 cases
Recall type: Voluntary: Firm initiated
Recalling firm: Gilster-Mary Lee Corporation

Original FDA data

Every field from FDA enforcement report F-0630-2019, exactly as published.

Show all FDA fields

City: Perryville
State: MO
Status: Terminated
Country: United States
Event ID: 81476
Address: 520 Old Saint Marys Rd
Code information: OCT 12 19 G9
Postal code: 63775-1835
Report date: Nov 28, 2018
Product type: Food
Recall number: F-0630-2019
Classification: Class II
Recalling firm: Gilster-Mary Lee Corporation
Product quantity: 221 cases
Termination date: Feb 5, 2019
Reason for recall: Buttered popcorn contains a milk ingredient (butter), but fails to declare milk on the label.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Microwave Movie Theater Butter Popcorn, Naturally Flavored, Net Wt. 19.8 OZ (1 lb 3.8 OZ), Distributed by Schnuck Markets, Inc. St. Louis, MO 63146
Distribution pattern: To one customer distribution center in Missouri.
Recall initiation date: Oct 31, 2018
Initial firm notification: E-Mail
Center classification date: Nov 16, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0630-2019, published Nov 28, 2018. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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