CLASS I Food recall · Reported 16 Sep 2020 · FDA Enforcement Report
Vegan Vanilla Cake recalled by Whole Foods Market
Whole Foods Market is recalling Vegan Vanilla Cake, distributed in Alabama, Florida, Georgia, Mississippi, North Carolina, Tennessee. The recall was initiated on 18 Aug 2020 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1430-2020
- FDA event ID
- 86277
- Recalling firm
- Whole Foods Market, Austin, TX
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 18 Aug 2020
- FDA classified
- 8 Sep 2020
- Reported
- 16 Sep 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Other
- Reason category
- Undeclared Soy
- Product category
- Cakes & Pastries
Timeline
| 18 Aug 2020 | Recall initiated by company | |
| 8 Sep 2020 | Classified by FDA | +21 days |
| 16 Sep 2020 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
undeclared soy (soy milk) allergen
Product as listed by the FDA
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
Where it was distributed
Alabama, Georgia, Mississippi, North Carolina, South Tennessee and one store in Tallahassee, Florida
AlabamaFloridaGeorgiaMississippiNorth CarolinaTennessee
Stores named: Whole Foods
Questions about this recall
Why was it recalled?
undeclared soy (soy milk) allergen
Which lots are affected?
PLU code of 41070 and product sell-by date through August 24, 2020.
Where was it sold?
Alabama, Georgia, Mississippi, North Carolina, South Tennessee and one store in Tallahassee, Florida
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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