Williams-Sonoma Recall: Williams Sonoma was notified by their contract manufacturer that high heat non fat dry milk powder that is now under recall for Salmonella was used in production of one of their quick bread mixes. - F-1236-2017
United States
TerminatedClass II
- Company
- Williams-Sonoma
- Product
- Williams-Sonoma Meyer Lemon Poppy Quick bread mix, NET WT. 1…
- Recall date
- December 13, 2016
- Terminated
- January 24, 2017
- Source
- FDA
Reason for recall
Williams Sonoma was notified by their contract manufacturer that high heat non fat dry milk powder that is now under recall for Salmonella was used in production of one of their quick bread mixes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Williams-Sonoma Meyer Lemon Poppy Quick bread mix, NET WT. 1 LB. 2 OZ (509 g) | Not published in this source record | 1220 units, 972 units currently at retail outlets | Lots: PO20710118, PO1351612, PO1351614, PO20710120. Best Before JAN2018 02118:A1 or Best Before JAN2018 02018:A1. |
Distribution
- Nationwide and one retail location in British Columbia
- Canada
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1236-2017
- Event ID
- 75985
- Status
- Terminated
- Classification
- Class II
- Company
- Williams-Sonoma
- Product description
- Williams-Sonoma Meyer Lemon Poppy Quick bread mix, NET WT. 1 LB. 2 OZ (509 g)
- Quantity
- 1220 units, 972 units currently at retail outlets
- Reason
- Williams Sonoma was notified by their contract manufacturer that high heat non fat dry milk powder that is now under recall for Salmonella was used in production of one of their quick bread mixes.
- Recall initiation date
- December 13, 2016
- Report date
- January 18, 2017
- Classification date
- Not published in this source record
- Termination date
- January 24, 2017
- Distribution pattern
- Nationwide and one retail location in British Columbia, Canada
- UPC, lot, and code information
- Lots: PO20710118, PO1351612, PO1351614, PO20710120. Best Before JAN2018 02118:A1 or Best Before JAN2018 02018:A1.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Williams-Sonoma
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 II mean?
FDA classifies this recall as Class II. 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.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
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 January 24, 2017.
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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