CLASS II Food recall · Reported 30 Apr 2014 · FDA Enforcement Report

Jolly Time Microwave popcorn, Extra Butter bags/carton recalled

American Pop Corn is recalling Jolly Time Microwave popcorn, Extra Butter bags/carton, distributed in 22 states. The recall was initiated on 11 Apr 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest By 03/31/15 (Julian date) 4090
Quantity recalled148 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-1884-2014
FDA event ID
68002
Recalling firm
American Pop Corn, Sioux City, IA
Classification
Class II
Status
Terminated
Recall initiated
11 Apr 2014
FDA classified
23 Apr 2014
Reported
30 Apr 2014
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Product category
Popcorn

Timeline

11 Apr 2014Recall initiated by company
23 Apr 2014Classified by FDA+12 days
30 Apr 2014Published in enforcement report+7 days

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

Reason for recall

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

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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.

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.

CaliforniaColoradoFloridaGeorgiaIowaIllinoisKansasKentuckyMassachusettsMichiganMissouriNebraskaNew JerseyNew YorkOhioOklahomaOregonPennsylvaniaSouth DakotaTexas

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

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.

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.

Other products in this recall event

2 other products · FDA event 68002

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