Class IITerminated in FDA datasetRecall initiated Oct 3, 2016

Hy Vee Long Johns (Red Raspberry Filled); Best If Used By 02/25/2017; Batch 162724690; NET WT…

Recalling firm: Mel-O Cream Donuts International, Inc.

Why it was recalled

Human fingertip found in product filling line.

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: Jul 21, 2017.

Check your package

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

ProductHy Vee Long Johns (Red Raspberry Filled); Best If Used By 02/25/2017; Batch 162724690; NET WT 14.63 Pounds; Approximate Unit Count: 72 units
Package size14.63 Pounds

FDA code information

Product Code: 63171; Batch 162724690; UPC: 4792403171; Best If Used By 02/25/2017

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

Full FDA record and distribution details

Original product description

Hy Vee Long Johns (Red Raspberry Filled); Best If Used By 02/25/2017; Batch 162724690; NET WT 14.63 Pounds; Approximate Unit Count: 72 units

Extracted codes and context

TypeCode / valueContext
best by02/25/2017Product Code: 63171; Batch 162724690; UPC: 4792403171; Best If Used By 02/25/2017
best by02/25/2017Hy Vee Long Johns (Red Raspberry Filled); Best If Used By 02/25/2017; Batch 162724690; NET WT 14.63 Pounds; Approximate Unit Count: 72 units

Original FDA recall reason

Human fingertip found in product filling line.

Recall details

Recall number
F-0546-2017
Event ID
75389
FDA status
Terminated
Initiated
Oct 3, 2016
Reported
Dec 7, 2016
Classified
Nov 25, 2016
Terminated
Jul 21, 2017
Quantity
3 cases
Location
Springfield, IL, 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

WI, IL, OH

FDA source record · F-0546-2017

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

Follow official FDA and manufacturer guidance.