Class IITerminated in FDA datasetRecall initiated Sep 5, 2013

12/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain

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 Plain, UPC 8-94700-01031-1; 6/16 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01037-3; 6/32 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01043-4
Package size6 oz
UPC894700010311, 894700010373, 894700010434

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 Plain, UPC 8-94700-01031-1; 6/16 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01037-3; 6/32 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01043-4

Extracted codes and context

TypeCode / valueContext
UPC89470001031112/6 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01031-1; 6/16 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01037-3; 6/32 oz. Chobani 2% Milkfat Low-Fat Gre
UPC894700010373C 8-94700-01031-1; 6/16 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01037-3; 6/32 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01043-4
UPC894700010434C 8-94700-01037-3; 6/32 oz. Chobani 2% Milkfat Low-Fat Greek Yogurt Plain, UPC 8-94700-01043-4

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-0013-2014
Event ID
66175
FDA status
Terminated
Initiated
Sep 5, 2013
Reported
Oct 30, 2013
Classified
Oct 21, 2013
Terminated
Nov 13, 2015
Quantity
1,954 (6 oz) cases; (16 oz) unknown cases; (32 oz) unknown 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-0013-2014

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

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