CLASS II Food recall · Reported 13 May 2015 · FDA Enforcement Report

Sunny Select Mango Guava recalled by Cott Beverages

Cott Beverages is recalling Sunny Select Mango Guava. The recall was initiated on 24 Feb 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUPC 7-17544-11799-5, Net Weight 1 L (12 singles p/c)
Quantity recalled6,486 CS (12/CS)

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-2177-2015
FDA event ID
70611
Recalling firm
Cott Beverages, Tampa, FL
Brand
Sunny
Classification
Class II
Status
Terminated
Recall initiated
24 Feb 2015
FDA classified
6 May 2015
Reported
13 May 2015
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Tree Nuts
Product category
Mangoes

Timeline

24 Feb 2015Recall initiated by company
6 May 2015Classified by FDA+71 days
13 May 2015Published in enforcement report+7 days

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

Reason for recall

May contain a trace amount of Tree Nuts (walnut) which is not listed in the ingredient list

Product as listed by the FDA

Sunny Select Mango Guava

Where it was distributed

US, Canada and Panama.

Questions about this recall

Is Sunny Select Mango Guava recalled?

Yes. Cott Beverages recalled Sunny Select Mango Guava on 24 Feb 2015. The recall is Class II and its status is Terminated. Recall number F-2177-2015.

Why was it recalled?

May contain a trace amount of Tree Nuts (walnut) which is not listed in the ingredient list

Which lots are affected?

UPC 7-17544-11799-5, Net Weight 1 L (12 singles p/c)

Where was it sold?

US, Canada and Panama.

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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