Class IITerminated in FDA datasetRecall initiated Sep 5, 2013

12/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended

Recalling firm: Chobani Idaho

Why it was recalled

Greek yogurt product Chobani brand is recalled due to report of illnesses and product bloated and swollen.

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: Nov 13, 2015.

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

Product12/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended, UPC 8-18290-01271-5; 6/4/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended-4 Value Pack, UPC 8-18290-01275-3
Package size6 oz
UPC818290012715, 818290012753

FDA code information

Sep 11-13 (four didit time stamp) to Oct 07-13 (four digit time stamp) 16-012. This code is interpreted as Best By dates September 11, 2013 through October 07, 2013; 16-012 is the IMS number of a production plant in Twin Falls, Idaho.

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Full FDA record and distribution details

Original product description

12/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended, UPC 8-18290-01271-5; 6/4/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended-4 Value Pack, UPC 8-18290-01275-3

Extracted codes and context

TypeCode / valueContext
UPC81829001271512/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended, UPC 8-18290-01271-5; 6/4/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended-4 Value Pack, UPC 8-18290-01275-3
UPC818290012753 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Key Lime Blended-4 Value Pack, UPC 8-18290-01275-3

Original FDA recall reason

Greek yogurt product Chobani brand is recalled due to report of illnesses and product bloated and swollen.

Recall details

Recall number
F-0062-2014
Event ID
66175
FDA status
Terminated
Initiated
Sep 5, 2013
Reported
Oct 30, 2013
Classified
Oct 21, 2013
Terminated
Nov 13, 2015
Quantity
56,578 cases
Location
Twin Falls, ID, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

distributed nationwide

FDA source record · F-0062-2014

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

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