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

Lot, batch or date codesC17102301 and C17121801
Quantity recalled10310 kg

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 2019Recall initiated by company
23 May 2019Classified by FDA+45 days
29 May 2019Published 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.

CaliforniaFloridaOhioTexas

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.

Other Other recalls

All 4,664