Class IITerminated in FDA datasetRecall initiated Jan 9, 2017

Holiday White Peppermint Hostess Twinkies, cream-filled snack cakes, Net Wt. 13.02 oz. (369 g)

Recalling firm: Hostess Brands, LLC

Why it was recalled

Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.

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.

ProductHoliday White Peppermint Hostess Twinkies, cream-filled snack cakes, Net Wt. 13.02 oz. (369 g), UPC 888109111571.
Package size13.02 oz
UPC888109111571

FDA code information

Batch and Best by Date per Material No. 701404: D093024000 12/4/2016 D100124000 12/5/2016 D100824000 12/12/2016 D101324000 12/17/2016 D101424000 12/18/2016 D102624000 12/30/2016 D102724000 12/31/2016 D110224000 1/6/2017 D110324000 1/7/2017 D110424000 1/8/2017 D111124000 1/15/2017 D111224000 1/16/2017 D112124000 1/25/2017; AND 701442 D100824000 12/12/2016 D102624000 12/30/2016 D110224000 1/6/2017 D111124000 1/15/2017 D112124000 1/25/2017

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

Full FDA record and distribution details

Original product description

Holiday White Peppermint Hostess Twinkies, cream-filled snack cakes, Net Wt. 13.02 oz. (369 g), UPC 888109111571.

Extracted codes and context

TypeCode / valueContext
UPC888109111571mint Hostess Twinkies, cream-filled snack cakes, Net Wt. 13.02 oz. (369 g), UPC 888109111571.

Original FDA recall reason

Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella.

Recall details

Recall number
F-1514-2017
Event ID
76184
FDA status
Terminated
Initiated
Jan 9, 2017
Reported
Mar 1, 2017
Classified
Feb 22, 2017
Terminated
Dec 1, 2017
Quantity
123,127 cases
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. There was no foreign/government/military distribution.

FDA source record · F-1514-2017

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

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