CLASS I Food recall · Reported 16 Aug 2017 · FDA Enforcement Report

Woodstock Organic Matcha Vanilla Oats cup recalled by Garden Of Light

Garden Of Light is recalling Woodstock Organic Matcha Vanilla Oats cup, distributed nationwide in the US. The recall was initiated on 14 Jul 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT CODES: MAY 11, 2018 & JUNE 23, 2018
Quantity recalled805 cases

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-3354-2017
FDA event ID
77767
Recalling firm
Garden Of Light, East Hartford, CT
Classification
Class I
Status
Terminated
Recall initiated
14 Jul 2017
FDA classified
4 Aug 2017
Reported
16 Aug 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Cereal

Timeline

14 Jul 2017Recall initiated by company
4 Aug 2017Classified by FDA+21 days
16 Aug 2017Published 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

Potential for Listeria contamination

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC: 0-42563-01786-6

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Potential for Listeria contamination

Which lots are affected?

LOT CODES: MAY 11, 2018 & JUNE 23, 2018

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 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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