CLASS II Food recall · Reported 28 Nov 2018 · FDA Enforcement Report

Microwave Movie Theater Butter Popcorn, Naturally Flavored recalled

Gilster-Mary Lee is recalling Microwave Movie Theater Butter Popcorn, Naturally Flavored, distributed in Missouri. The recall was initiated on 31 Oct 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesOCT 12 19 G9
Quantity recalled221 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0630-2019
FDA event ID
81476
Recalling firm
Gilster-Mary Lee, Perryville, MO
Classification
Class II
Status
Terminated
Recall initiated
31 Oct 2018
FDA classified
16 Nov 2018
Reported
28 Nov 2018
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Milk
Product category
Popcorn

Timeline

31 Oct 2018Recall initiated by company
16 Nov 2018Classified by FDA+16 days
28 Nov 2018Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

To one customer distribution center in Missouri.

Missouri

Questions about this recall

Why was it recalled?

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

Which lots are affected?

OCT 12 19 G9

Where was it sold?

To one customer distribution center in Missouri.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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