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Class II: temporary or reversible health riskTerminated

Hostess Donettes Powdered Mini Donuts Recall

Hostess Donettes Powdered Mini Donuts, packaged in 9ct and 6-20ct bags of mini donuts

Hostess Brands, LLC · Kansas City, MO

Risk level
Class II
Reported by FDA
Sep 21, 2016
Recall ID
F-2119-2016
Check your lot numberHow we source this data

Summary

Hostess Brands recalled Hostess Donettes Powdered Mini Donuts starting Jun 3, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2119-2016 on Sep 21, 2016. Reason: Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts. Status: Terminated.

Why it was recalled

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

Product description

Hostess Donettes Powdered Mini Donuts, packaged in 9ct and 6-20ct bags of mini donuts, net wt. 10.5oz, UPC 888109150044; packaged in 9ct bag of mini donuts, net wt. 13.16oz, UPC 888109110246; packaged in 6ct single serve packages, net wt. 3oz, UPC 888109050047; the most responsible firm on the label is Hostess Brands, LLC, Kansas City, MO 64141

Lot numbers, UPCs & expiration codes

batch and best by date per UPC code: UPC 888109110246: D031921000, best by 5/23/2016 D032021000, best by 5/24/2016 D032121000, best by 5/25/2016 D040821000, best by 6/12/2016 UPC 888109150044: D031821000, best by 5/22/2016 D031821001, best by 6/8/2016 D031824000, best by 6/8/2016 D031921000, best by 5/23/2016 D031921001, best by 6/8/2016 D040221000, best by 6/6/2016 D040821000, best by 6/12/2016 D032121000, best by 5/25/2016 UPC 888109050047: D031821000, best by 5/22/2016 D031921000, best by 5/23/2016 D040221000, best by 6/6/2016 D040821000, best by 6/12/2016

Where it was sold

Nationwide distribution. No foreign or military/government distribution.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2119-2016
Classification
Class II
Status
Terminated
Recall initiated
Jun 3, 2016
FDA report date
Sep 21, 2016
Quantity
1,294,627 units
Recall type
Voluntary: Firm initiated
Recalling firm
Hostess Brands, LLC

Original FDA data

Every field from FDA enforcement report F-2119-2016, exactly as published.

Show all FDA fields
City
Kansas City
State
MO
Status
Terminated
Country
United States
Event ID
74287
Address
1 E Armour Blvd
Code information
batch and best by date per UPC code: UPC 888109110246: D031921000, best by 5/23/2016 D032021000, best by 5/24/2016 D032121000, best by 5/25/2016 D040821000, best by 6/12/2016 UPC 888109150044: D031821000, best by 5/22/2016 D031821001, best by 6/8/2016 D031824000, best by 6/8/2016 D031921000, best by 5/23/2016 D031921001, best by 6/8/2016 D040221000, best by 6/6/2016 D040821000, best by 6/12/2016 D032121000, best by 5/25/2016 UPC 888109050047: D031821000, best by 5/22/2016 D031921000, best by 5/23/2016 D040221000, best by 6/6/2016 D040821000, best by 6/12/2016
Postal code
64111-1201
Report date
Sep 21, 2016
Product type
Food
Recall number
F-2119-2016
Classification
Class II
Recalling firm
Hostess Brands, LLC
Product quantity
1,294,627 units
Termination date
Dec 1, 2017
Reason for recall
Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Hostess Donettes Powdered Mini Donuts, packaged in 9ct and 6-20ct bags of mini donuts, net wt. 10.5oz, UPC 888109150044; packaged in 9ct bag of mini donuts, net wt. 13.16oz, UPC 888109110246; packaged in 6ct single serve packages, net wt. 3oz, UPC 888109050047; the most responsible firm on the label is Hostess Brands, LLC, Kansas City, MO 64141
Distribution pattern
Nationwide distribution. No foreign or military/government distribution.
Recall initiation date
Jun 3, 2016
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Sep 13, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2119-2016, published Sep 21, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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