CLASS II Food recall · Reported 2 Sep 2020 · FDA Enforcement Report
Buttermilk Biscuits recalled by Whole Foods Market
Whole Foods Market is recalling Buttermilk Biscuits, distributed in Alabama, Georgia, Mississippi, North Carolina, South Carolina, Tennessee. The recall was initiated on 6 Aug 2020 and the FDA has classified it as Class II.
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-1257-2020
- FDA event ID
- 86275
- Recalling firm
- Whole Foods Market, Austin, TX
- Brand
- Buttermilk Biscuits
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Aug 2020
- FDA classified
- 21 Aug 2020
- Reported
- 2 Sep 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Soy
- Product category
- Oysters & Shellfish
Timeline
| 6 Aug 2020 | Recall initiated by company | |
| 21 Aug 2020 | Classified by FDA | +15 days |
| 2 Sep 2020 | Published in enforcement report | +12 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 allergen
Product as listed by the FDA
Whole Foods Market Buttermilk Biscuits, 4pk NET WT 1lb 0 oz PLU: 30561 packaged in plastic clam shell
Where it was distributed
North Carolina, Alabama, South Carolina, Georgia, Tennessee, Mississippi
AlabamaGeorgiaMississippiNorth CarolinaSouth CarolinaTennessee
Stores named: Whole Foods
Questions about this recall
Why was it recalled?
Undeclared soy allergen
Which lots are affected?
Sell though 8/8/20
Where was it sold?
North Carolina, Alabama, South Carolina, Georgia, Tennessee, Mississippi
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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