Class IITerminated in FDA datasetRecall initiated Jun 3, 2016

Hostess Donettes Double Chocolate Mini Donuts, packaged in 9-ct bags of mini donuts, net wt.…

Recalling firm: Hostess Brands, LLC

Why it was recalled

Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.

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: Dec 1, 2017.

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

ProductHostess Donettes Double Chocolate Mini Donuts, packaged in 9-ct bags of mini donuts, net wt. 11.25 oz, UPC 888109150037, the most responsible firm name on the label is Hostess Brands, LLC in Kansas City,MO 64141.
Package size11.25 oz
UPC888109150037

FDA code information

UPC 888109150037: D040221000, best by 6/6/2016 D040821000, best by 6/12/2016

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Full FDA record and distribution details

Original product description

Hostess Donettes Double Chocolate Mini Donuts, packaged in 9-ct bags of mini donuts, net wt. 11.25 oz, UPC 888109150037, the most responsible firm name on the label is Hostess Brands, LLC in Kansas City,MO 64141.

Extracted codes and context

TypeCode / valueContext
UPC888109150037UPC 888109150037: D040221000, best by 6/6/2016 D040821000, best by 6/12/2016
UPC888109150037colate Mini Donuts, packaged in 9-ct bags of mini donuts, net wt. 11.25 oz, UPC 888109150037, the most responsible firm name on the label is Hostess Brands, LLC in Kansas City,MO 64141.
best by6/12/2016UPC 888109150037: D040221000, best by 6/6/2016 D040821000, best by 6/12/2016
best by6/6/2016UPC 888109150037: D040221000, best by 6/6/2016 D040821000, best by 6/12/2016

Original FDA recall reason

Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.

Recall details

Recall number
F-2120-2016
Event ID
74287
FDA status
Terminated
Initiated
Jun 3, 2016
Reported
Sep 21, 2016
Classified
Sep 13, 2016
Terminated
Dec 1, 2017
Quantity
95,769 units
Location
Kansas City, MO, 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

Nationwide distribution. No foreign or military/government distribution.

FDA source record · F-2120-2016

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

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