Class ITerminated in FDA datasetRecall initiated Jun 4, 2013

General Mills, Cinnamon Toast Crunch, 25% Less Sugar, Self-Serve Bowl, Net WT 1.0 oz ( 28g)

Recalling firm: General Mills, Inc

Why it was recalled

General Mills is recalling a small quantity of single-serve reduced-sugar Cinnamon Toast Crunch bowlpak sold in foodservice establishments. The company was notified by an…

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: Mar 31, 2014.

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ProductGeneral Mills, Cinnamon Toast Crunch, 25% Less Sugar, Self-Serve Bowl, Net WT 1.0 oz ( 28g), Distributed by General Mills Sales, Minneapolis, MN 55440, Package UPC 00016000294448. Case: General Mills, BOWLPAK, Cinnamon Toast Crunch, Reduced Sugar, 96 - 1 oz (28g) containers, Distributed by General Mills Sales, Minneapolis, MN 55440, Case UPC 10016000294445.
Package size1.0 oz

FDA code information

Better if Used By: Case Date Code: 31AUG2013, 02SEP2013

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Full FDA record and distribution details

Original product description

General Mills, Cinnamon Toast Crunch, 25% Less Sugar, Self-Serve Bowl, Net WT 1.0 oz ( 28g), Distributed by General Mills Sales, Minneapolis, MN 55440, Package UPC 00016000294448. Case: General Mills, BOWLPAK, Cinnamon Toast Crunch, Reduced Sugar, 96 - 1 oz (28g) containers, Distributed by General Mills Sales, Minneapolis, MN 55440, Case UPC 10016000294445.

Original FDA recall reason

General Mills is recalling a small quantity of single-serve reduced-sugar Cinnamon Toast Crunch bowlpak sold in foodservice establishments. The company was notified by an ingredient supplier that it had recalled an ingredient due to the possible presence of salmonella.

Recall details

Recall number
F-1589-2013
Event ID
65363
FDA status
Terminated
Initiated
Jun 4, 2013
Reported
Jul 10, 2013
Classified
Jul 2, 2013
Terminated
Mar 31, 2014
Quantity
168 cases ( 96 individual 1.0 oz bowlpacks)
Location
Minneapolis, MN, 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

The recall involved 2 customers with 6 shipping locations. WV, SC, VA, GA, TN.

FDA source record · F-1589-2013

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

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