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Class IITerminated in FDA datasetRecall initiated Apr 11, 2014

Jolly Time Microwave popcorn, Extra Butter, 3/3-oz bags/carton. The cartons are packaged…

Recalling firm: American Pop Corn Co

Why it was recalled

Possible metal fragments

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jul 28, 2014.

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

ProductJolly Time Microwave popcorn, Extra Butter, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190008477, on the 12 count case - UPC 10028190008474 and 48 ct shipper with UPC 128190488474 American Pop Corn Company, Sioux City, IA.
UPC028190008477, 128190488474

FDA code information

Best By 03/31/15 (Julian date) 4090

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Full FDA record and distribution details

Original product description

Jolly Time Microwave popcorn, Extra Butter, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190008477, on the 12 count case - UPC 10028190008474 and 48 ct shipper with UPC 128190488474 American Pop Corn Company, Sioux City, IA.

Extracted codes and context

TypeCode / valueContext
UPC028190008477 bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190008477, on the 12 count case - UPC 10028190008474 and 48 ct shipper with UPC 128190488474 American Pop Corn Company, Sioux
UPC128190488474190008477, on the 12 count case - UPC 10028190008474 and 48 ct shipper with UPC 128190488474 American Pop Corn Company, Sioux City, IA.
best by03/31/15Best By 03/31/15 (Julian date) 4090

Original FDA recall reason

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

Recall details

Recall number
F-1884-2014
Event ID
68002
FDA status
Terminated
Initiated
Apr 11, 2014
Reported
Apr 30, 2014
Classified
Apr 23, 2014
Terminated
Jul 28, 2014
Quantity
148 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-1884-2014

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

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