Class IITerminated in FDA datasetRecall initiated Jun 3, 2016

Hostess Donettes Maple Glazed Mini Donuts, packaged in 9-17-ct bagsof 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.

Check your package

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

ProductHostess Donettes Maple Glazed Mini Donuts, packaged in 9-17-ct bagsof mini donuts, net wt. 10.50oz, UPC 888109111243; the most responsible firm name on the label is Hostess Brands LLC, Kansas City, MO 64141.
Package size10.50oz
UPC888109111243

FDA code information

UPC code 888109111243: D032424000, best by 5/28/2016

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 Maple Glazed Mini Donuts, packaged in 9-17-ct bagsof mini donuts, net wt. 10.50oz, UPC 888109111243; the most responsible firm name on the label is Hostess Brands LLC, Kansas City, MO 64141.

Extracted codes and context

TypeCode / valueContext
UPC888109111243UPC code 888109111243: D032424000, best by 5/28/2016
UPC888109111243lazed Mini Donuts, packaged in 9-17-ct bagsof mini donuts, net wt. 10.50oz, UPC 888109111243; the most responsible firm name on the label is Hostess Brands LLC, Kansas City, MO 64141.
best by5/28/2016UPC code 888109111243: D032424000, best by 5/28/2016

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-2123-2016
Event ID
74287
FDA status
Terminated
Initiated
Jun 3, 2016
Reported
Sep 21, 2016
Classified
Sep 13, 2016
Terminated
Dec 1, 2017
Quantity
26,289 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-2123-2016

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

Follow official FDA and manufacturer guidance.