CLASS II Food recall · Reported 20 Jan 2016 · FDA Enforcement Report

Sweet Leaf Organic Raspberry Iced Tea recalled

Nestle Waters North America is recalling Sweet Leaf Organic Raspberry Iced Tea, distributed nationwide in the US. The recall was initiated on 9 Dec 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest By Dates: 6/30/16, 8/31/16, 10/31/16
Quantity recalled13,175 cases (12/case)

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-0502-2016
FDA event ID
72821
Recalling firm
Nestle Waters North America, Stamford, CT
Classification
Class II
Status
Terminated
Recall initiated
9 Dec 2015
FDA classified
12 Jan 2016
Reported
20 Jan 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Particulate Matter
Product category
Tea

Timeline

9 Dec 2015Recall initiated by company
12 Jan 2016Classified by FDA+34 days
20 Jan 2016Published in enforcement report+8 days

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

Reason for recall

Product contains glass particles

Product as listed by the FDA

Sweet Leaf Organic Raspberry Iced Tea, 16 oz glass bottle UPC: 6-51538-06703-6

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Sweet Leaf Organic Raspberry Iced Tea recalled?

Yes. Nestle Waters North America recalled Sweet Leaf Organic Raspberry Iced Tea on 9 Dec 2015. The recall is Class II and its status is Terminated. Recall number F-0502-2016.

Why was it recalled?

Product contains glass particles

Which lots are affected?

Best By Dates: 6/30/16, 8/31/16, 10/31/16

Where was it sold?

Nationwide

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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