CLASS I Food recall · Reported 11 Nov 2015 · FDA Enforcement Report

Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola recalled

Greencore USA is recalling Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola, distributed in 7 states. The recall was initiated on 22 Sep 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesEnjoy by 9/24
Quantity recalled994 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0123-2016
FDA event ID
72257
Recalling firm
Greencore USA, North Kingstown, RI
Classification
Class I
Status
Terminated
Recall initiated
22 Sep 2015
FDA classified
30 Oct 2015
Reported
11 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Tree Nuts
Product category
Granola Bars

Timeline

22 Sep 2015Recall initiated by company
30 Oct 2015Classified by FDA+38 days
11 Nov 2015Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product may contain undeclared almonds.

Product as listed by the FDA

Evolution Fresh Nonfat Greek Yogurt with Strawberry and Granola, 6.1oz., UPC: 7 6211107474 4

Where it was distributed

266 Starbucks retail stores in Massachusetts, Rhode Island, New Hampshire, New York, Connecticut, Vermont and Maine.

ConnecticutMassachusettsMaineNew HampshireNew YorkRhode IslandVermont

Stores named: Starbucks

Questions about this recall

Why was it recalled?

Product may contain undeclared almonds.

Which lots are affected?

Enjoy by 9/24

Where was it sold?

266 Starbucks retail stores in Massachusetts, Rhode Island, New Hampshire, New York, Connecticut, Vermont and Maine.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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