FDA Recall United States TerminatedTerminated: August 16, 2018Historical recordClass II
Garden Of Light Inc.
- Product
- (a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch,…
- Published
- September 6, 2017
- Distribution
- Nationwide
Garden Of Light Inc. Recall: Potential for Listeria contamination - F-3354-2017
United States
TerminatedClass I
- Company
- Garden Of Light Inc.
- Product
- WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC…
- Recall date
- July 14, 2017
- Terminated
- June 19, 2018
- Source
- FDA
Reason for recall
Potential for Listeria contamination
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC: 0-42563-01786-6 | 0-42563-01786-6 | 805 cases | LOT CODES: MAY 11, 2018 & JUNE 23, 2018 |
Distribution
- Nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-3354-2017
- Event ID
- 77767
- Status
- Terminated
- Classification
- Class I
- Company
- Garden Of Light Inc.
- Product description
- WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC: 0-42563-01786-6
- Quantity
- 805 cases
- Reason
- Potential for Listeria contamination
- Recall initiation date
- July 14, 2017
- Report date
- August 16, 2017
- Classification date
- Not published in this source record
- Termination date
- June 19, 2018
- Distribution pattern
- Nationwide
- UPC, lot, and code information
- UPC 0-42563-01786-6; LOT CODES: MAY 11, 2018 & JUNE 23, 2018
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Garden Of Light Inc.
Other recalls from Garden Of Light Inc.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of June 19, 2018.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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