Class IITerminated in FDA datasetApr 11, 2014

Jolly Time Microwave popcorn, Homemade Classic Stovetop Flavor, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton -

Recalling firm: American Pop Corn Co

Why it was recalled

The product has the potential to be contaminated with stainless steel metal fragments.

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Compare the exact product and package details with the label you have.

ProductJolly Time Microwave popcorn, Homemade Classic Stovetop Flavor, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190007807, on the 12-ct case - UPC 10028190007804, 48-ct shipper UPC 128190487804 American Pop Corn Company, Sioux City, IA
UPC028190007807, 128190487804

FDA code information

Best By code of 04/01/15 (Julian date) 4091

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Full FDA record and distribution details

Original product description

Jolly Time Microwave popcorn, Homemade Classic Stovetop Flavor, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190007807, on the 12-ct case - UPC 10028190007804, 48-ct shipper UPC 128190487804 American Pop Corn Company, Sioux City, IA

Extracted codes and context

TypeCode / valueContext
UPC028190007807ags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190007807, on the 12-ct case - UPC 10028190007804, 48-ct shipper UPC 128190487804 American Pop Corn Company, Sioux City, IA
UPC128190487804n - UPC 028190007807, on the 12-ct case - UPC 10028190007804, 48-ct shipper UPC 128190487804 American Pop Corn Company, Sioux City, IA

Recall details

Recall number
F-1885-2014
Event ID
68002
FDA status
Terminated
Initiated
Apr 11, 2014
Reported
Apr 30, 2014
Classified
Apr 23, 2014
Terminated
Jul 28, 2014
Quantity
103 cases
Location
Sioux City, IA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Distribution was made to CA, CO, FL, GA, IA, IL, KS, KY, MA, MI, MO, NE, NJ, NY, OH, OK, OR, PA, SD, TX, WA and WI.

FDA source record · F-1885-2014

Data updated September 16, 2026. View official FDA data ↗

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