Class ITerminated in FDA datasetRecall initiated Sep 23, 2016

Frozen Onion Rings sold and distributed under the following private label retail brands: 1)…

Recalling firm: McCain Foods USA

Why it was recalled

Product label does not declare milk.

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: Apr 25, 2017.

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ProductFrozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and Match Onion Rings, NET WT 40 OZ, packaged in plastic bags; 2) Krasdale Onion Rings, NET WT 16 OZ, packaged in plastic bags; 3) Spartan Onion Rings, NET WT 20 OZ, packaged in plastic bags; 4) Shur Fine Onion Rings, NET WT. 16 OZ, packaged in plastic bags; 5) Kroger Onion Rings, NET WT. 20 OZ, packaged in plastic bags; and 6) Fareway Breaded Onion Rings, NET WT. 20 OZ, packaged in plastic bags.
Package size40 OZ

FDA code information

Product manufactured after October 20, 2015 and prior to September 23, 2016 with production date codes: V151020 through V160923.

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Full FDA record and distribution details

Original product description

Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and Match Onion Rings, NET WT 40 OZ, packaged in plastic bags; 2) Krasdale Onion Rings, NET WT 16 OZ, packaged in plastic bags; 3) Spartan Onion Rings, NET WT 20 OZ, packaged in plastic bags; 4) Shur Fine Onion Rings, NET WT. 16 OZ, packaged in plastic bags; 5) Kroger Onion Rings, NET WT. 20 OZ, packaged in plastic bags; and 6) Fareway Breaded Onion Rings, NET WT. 20 OZ, packaged in plastic bags.

Original FDA recall reason

Product label does not declare milk.

Recall details

Recall number
F-0433-2017
Event ID
75280
FDA status
Terminated
Initiated
Sep 23, 2016
Reported
Nov 23, 2016
Classified
Nov 15, 2016
Terminated
Apr 25, 2017
Quantity
1) 29,956 cases; 2) 1,318 cases; 3) 5,087 cases; 4) 4,313 cases; 5) 16,440 cases; 6) 2,200 cases
Location
Lisle, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Recalled product was distributed to direct accounts in AL, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MD, MI, MO, NC, NE, NY, OH, TN, TX, VA, and WI

FDA source record · F-0433-2017

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

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