WFM Purchasing, LP food recall: Whole Foods Market Blueberry Almond Granola
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97644
- Recall initiated
- Sep 9, 2025
- Classified by FDA
- Oct 2, 2025
- Posted in Enforcement Report
- Oct 8, 2025
- Terminated
- Oct 1, 2026
- Recalling firm
- WFM Purchasing, LP
- Firm location
- Austin, TX, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Product was incorrectly labeled, resulting in undeclared wheat, sesame, and cashew.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Sep 9, 2025. FDA classified it 23 days later, on Oct 2, 2025. Distribution reported by FDA: One retail store in Philadelphia, PA. WFM Purchasing, LP has 5 recalls in our records.
Recalled products (1)
H-0002-2026 Class I Terminated
Whole Foods Market Blueberry Almond Granola, PLU 86032, packaged in a clear plastic container.
Codes / lots: Packed On 09/01/2025 Sell By 11/30/2025
Quantity: 6 units (1 pound each)
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 97644
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.