Class IITerminated in FDA datasetRecall initiated Jul 21, 2015

KellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO:…

Recalling firm: Kellbran Candies and Snacks Inc

Why it was recalled

The firm was notified by the Ohio Dept. of Agriculture of possible mislabeling with their Allergen declaration of 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: Oct 19, 2015.

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ProductKellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO: Manufactured in a facility that processes peanuts, nuts, soy and milk. UPC 0 96637 50153 9 kellbrancandies.com KellBran Candies, Inc. Akron, Ohio 44312
Package size8 oz
UPC096637501539

FDA code information

Best Used By: 11/30/2015 Lot 181317 4 & Best Used By: 12/31/2015 211830 6

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Full FDA record and distribution details

Original product description

KellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO: Manufactured in a facility that processes peanuts, nuts, soy and milk. UPC 0 96637 50153 9 kellbrancandies.com KellBran Candies, Inc. Akron, Ohio 44312

Extracted codes and context

TypeCode / valueContext
UPC096637501539NFO: Manufactured in a facility that processes peanuts, nuts, soy and milk. UPC 0 96637 50153 9 kellbrancandies.com KellBran Candies, Inc. Akron, Ohio 44312
best by11/30/2015Best Used By: 11/30/2015 Lot 181317 4 & Best Used By: 12/31/2015 211830 6
best by12/31/2015Best Used By: 11/30/2015 Lot 181317 4 & Best Used By: 12/31/2015 211830 6

Original FDA recall reason

The firm was notified by the Ohio Dept. of Agriculture of possible mislabeling with their Allergen declaration of undeclared milk.

Recall details

Recall number
F-3226-2015
Event ID
71753
FDA status
Terminated
Initiated
Jul 21, 2015
Reported
Sep 23, 2015
Classified
Sep 11, 2015
Terminated
Oct 19, 2015
Quantity
150cs/40/8 oz bags
Location
Akron, OH, 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

Product was shipped to the following states: AL, AR, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MO, MS, NC, NH, NJ, NY, OH, OK, PA, SC, TN, TX, VA & WI.

FDA source record · F-3226-2015

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

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