Class ITerminated in FDA datasetRecall initiated Apr 26, 2013

Orville Redenbacher's Classic Kettle Korn, sweet and salty popcorn, ready-to-eat, packaged in…

Recalling firm: Conagra Inc

Why it was recalled

The kettle korn flavored ready-to-eat popcorn product may contain ready-to-eat white cheddar flavored popcorn which may pose a hazard to health due to undeclared milk.

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: May 28, 2014.

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

ProductOrville Redenbacher's Classic Kettle Korn, sweet and salty popcorn, ready-to-eat, packaged in 5-oz/plastic bags (Unit UPC code 027000523216) and 1.5-oz/plastic bags (Unit UPC code 027000523254).
UPC027000523216, 027000523254

FDA code information

5-oz bags: Batch Code 5486234100, Best by Date SEP 02 2013; Batch Code 5486234200, Best by Date SEP 03 2013; and Batch Code 5486234300, Best by Date SEP 04 2013. 1.5-oz bags: Batch Code 5486234200, Best by Date SEP 03 2013 and Batch Code 5486234300, Best by Date SEP 04 2013.

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Full FDA record and distribution details

Original product description

Orville Redenbacher's Classic Kettle Korn, sweet and salty popcorn, ready-to-eat, packaged in 5-oz/plastic bags (Unit UPC code 027000523216) and 1.5-oz/plastic bags (Unit UPC code 027000523254).

Extracted codes and context

TypeCode / valueContext
UPC027000523216t and salty popcorn, ready-to-eat, packaged in 5-oz/plastic bags (Unit UPC code 027000523216) and 1.5-oz/plastic bags (Unit UPC code 027000523254).
UPC027000523254lastic bags (Unit UPC code 027000523216) and 1.5-oz/plastic bags (Unit UPC code 027000523254).

Original FDA recall reason

The kettle korn flavored ready-to-eat popcorn product may contain ready-to-eat white cheddar flavored popcorn which may pose a hazard to health due to undeclared milk.

Recall details

Recall number
F-1443-2013
Event ID
65035
FDA status
Terminated
Initiated
Apr 26, 2013
Reported
May 29, 2013
Classified
May 22, 2013
Terminated
May 28, 2014
Quantity
8,666/8/5-oz bag/cases and 5,707/8/1.5-oz bag/cases
Location
Omaha, NE, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distribution was made nationwide.

FDA source record · F-1443-2013

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

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