FDA Recall United States Terminated Historical 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
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.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
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?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
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.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
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