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WHOLE FOODS MARKET Recall: undeclared soy (soy milk) allergen

United States

TerminatedClass I

Company
WHOLE FOODS MARKET
Product
Whole Foods Market Vegan Vanilla Cake 6 Inch NET WT 2lb 11oz…
Recall date
August 18, 2020
Terminated
November 3, 2020
Source
FDA

Reason for recall

undeclared soy (soy milk) allergen

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Whole Foods Market Vegan Vanilla Cake 6 Inch NET WT 2lb 11oz (1219g) Packed for Whole Foods Market PLU 41070 packaged in plastic dome containers with Whole Foods Market scale labels Not published in this source record 18 units PLU code of 41070 and product sell-by date through August 24, 2020.

Distribution

  • Alabama
  • Georgia
  • Mississippi
  • North Carolina
  • South Tennessee and one store in Tallahassee
  • Florida

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1430-2020
Event ID
86277
Status
Terminated
Classification
Class I
Company
WHOLE FOODS MARKET
Product description
Whole Foods Market Vegan Vanilla Cake 6 Inch NET WT 2lb 11oz (1219g) Packed for Whole Foods Market PLU 41070 packaged in plastic dome containers with Whole Foods Market scale labels
Quantity
18 units
Reason
undeclared soy (soy milk) allergen
Recall initiation date
August 18, 2020
Report date
September 16, 2020
Classification date
Not published in this source record
Termination date
November 3, 2020
Distribution pattern
Alabama, Georgia, Mississippi, North Carolina, South Tennessee and one store in Tallahassee, Florida
UPC, lot, and code information
PLU code of 41070 and product sell-by date through August 24, 2020.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Other
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: WHOLE FOODS MARKET

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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?

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.