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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.

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.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
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
E-Mail
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.

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.