CLASS III Food recall · Reported 29 May 2019 · FDA Enforcement Report
Goji Powder (aka Wolfberry Powder) recalled by Xi'an Yuensun Biological
Xi'an Yuensun Biological Technology is recalling Goji Powder (aka Wolfberry Powder), distributed in California, Florida, Ohio, Texas. The recall was initiated on 8 Apr 2019 and the FDA has classified it as Class III.
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-1397-2019
- FDA event ID
- 82735
- Recalling firm
- Xi'an Yuensun Biological Technology, Xi'An, N/A
- Brand
- Goji
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 8 Apr 2019
- FDA classified
- 23 May 2019
- Reported
- 29 May 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Other
Timeline
| 8 Apr 2019 | Recall initiated by company | |
| 23 May 2019 | Classified by FDA | +45 days |
| 29 May 2019 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Fungicide carbendazim found in product.
Product as listed by the FDA
Goji Powder (aka Wolfberry Powder)
Where it was distributed
U.S. distribution to the following: CA, OH, TX, and FL Foreign distribution to the following: China, Indonesia, Korea, and Australia.
Questions about this recall
Why was it recalled?
Fungicide carbendazim found in product.
Which lots are affected?
C17102301 and C17121801
Where was it sold?
U.S. distribution to the following: CA, OH, TX, and FL Foreign distribution to the following: China, Indonesia, Korea, and Australia.
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 III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
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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