Class IITerminated in FDA datasetRecall initiated Jun 3, 2016

Hostess Donettes Glazed Mini Donuts, packaged in 9-17-ct and 6-17-ct bags of mini donuts, net…

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 Glazed Mini Donuts, packaged in 9-17-ct and 6-17-ct bags of mini donuts, net wt. 10.50oz, UPC 888109110659;the most responsible firm name on the label is Hostess Brands, LLC, Kansas City, MO 64141.
Package size10.50oz
UPC888109110659

FDA code information

UPC 888109110659 D032124000, best by 5/25/2016 D032824000, best by 6/1/2016 D032924000, best by 6/2/2016 D041124000, best by 6/15/2016 D041224000, best by 6/16/2016 D032224000, best by 5/26/2016 D032324000, best by 5/27/2016 D032424000, best by 5/28/2016 D041324000, best by 6/17/2016 D041424000, best by 6/18/2016

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Hostess Donettes Glazed Mini Donuts, packaged in 9-17-ct and 6-17-ct bags of mini donuts, net wt. 10.50oz, UPC 888109110659;the most responsible firm name on the label is Hostess Brands, LLC, Kansas City, MO 64141.

Extracted codes and context

TypeCode / valueContext
UPC888109110659UPC 888109110659 D032124000, best by 5/25/2016 D032824000, best by 6/1/2016 D032924000, best by 6/2/2016 D041124000, best by 6/15/
UPC888109110659nuts, packaged in 9-17-ct and 6-17-ct bags of mini donuts, net wt. 10.50oz, UPC 888109110659;the most responsible firm name on the label is Hostess Brands, LLC, Kansas City, MO 64141.
best by5/25/2016UPC 888109110659 D032124000, best by 5/25/2016 D032824000, best by 6/1/2016 D032924000, best by 6/2/2016 D041124000, best by 6/15/2016 D041224000, best by 6/16/20
best by5/26/201641124000, best by 6/15/2016 D041224000, best by 6/16/2016 D032224000, best by 5/26/2016 D032324000, best by 5/27/2016 D032424000, best by 5/28/2016 D041324000, best by 6/17/2016 D041424000, best by 6/18/
best by5/27/201641224000, best by 6/16/2016 D032224000, best by 5/26/2016 D032324000, best by 5/27/2016 D032424000, best by 5/28/2016 D041324000, best by 6/17/2016 D041424000, best by 6/18/2016
best by5/28/201632224000, best by 5/26/2016 D032324000, best by 5/27/2016 D032424000, best by 5/28/2016 D041324000, best by 6/17/2016 D041424000, best by 6/18/2016
best by6/1/2016UPC 888109110659 D032124000, best by 5/25/2016 D032824000, best by 6/1/2016 D032924000, best by 6/2/2016 D041124000, best by 6/15/2016 D041224000, best by 6/16/2016 D032224000, best by 5/26/2
best by6/15/2016D032824000, best by 6/1/2016 D032924000, best by 6/2/2016 D041124000, best by 6/15/2016 D041224000, best by 6/16/2016 D032224000, best by 5/26/2016 D032324000, best by 5/27/2016 D032424000, best by 5/28/
best by6/16/2016032924000, best by 6/2/2016 D041124000, best by 6/15/2016 D041224000, best by 6/16/2016 D032224000, best by 5/26/2016 D032324000, best by 5/27/2016 D032424000, best by 5/28/2016 D041324000, best by 6/17/
best by6/17/201632324000, best by 5/27/2016 D032424000, best by 5/28/2016 D041324000, best by 6/17/2016 D041424000, best by 6/18/2016
best by6/18/201632424000, best by 5/28/2016 D041324000, best by 6/17/2016 D041424000, best by 6/18/2016
best by6/2/2016032124000, best by 5/25/2016 D032824000, best by 6/1/2016 D032924000, best by 6/2/2016 D041124000, best by 6/15/2016 D041224000, best by 6/16/2016 D032224000, best by 5/26/2016 D032324000, best by 5/27/

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-2122-2016
Event ID
74287
FDA status
Terminated
Initiated
Jun 3, 2016
Reported
Sep 21, 2016
Classified
Sep 13, 2016
Terminated
Dec 1, 2017
Quantity
505,704 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-2122-2016

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

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