Hostess Donettes Glazed Mini Donuts, packaged in 9-17-ct and 6-17-ct bags of mini…
Hostess Brands, LLC recalled this product and the FDA reported the enforcement action on 21 September 2016 as Class II. The recall was initiated by the firm. Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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.
- UPC
- 888109110659
- Reason for recall
- Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
- Recalling firm
- Hostess Brands, LLC
- Firm location
- Kansas City, Missouri, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-2122-2016
- Quantity
- 505,704 units
- Distribution
- Nationwide distribution. No foreign or military/government distribution.
- Initiated
- 3 June 2016
- Reported by FDA
- 21 September 2016
- Terminated
- 1 December 2017
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- 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
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 11 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 11 separate recalls, which almost every published figure does, overstates it by a factor of 11. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 11 of them.
- The recall ran for 18 months, from 3 June 2016 to termination on 1 December 2017. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The FDA published the enforcement report 4 months after the firm began the recall.
- Recalls of a bakery product run a median of 6 months, so this one was longer than usual for its category. Bakery is overwhelmingly an allergen category rather than a pathogen one: baking is a kill step, but a bakery runs many recipes down shared lines, so the failure that recalls a bakery product is usually a label or a changeover.
Filed under bakery. A product can sit in more than one.
Other bakery recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Hostess Brands, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 22 other records name this firm.
All 23 records for Hostess Brands, LLC
All 2016 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.