📍Recalling firmXi'an Yuensun Biological Technology Co., Ltd.No. 2 Datang Power Plant Extension End, Yuxia Town · Xi'An, China
✎ GovInfoNow plain-language explainer
Xi'an Yuensun Biological Technology Co., Ltd. is recalling Goji Powder (Wolfberry Powder) because it contains the fungicide carbendazim. This chemical poses a health risk, so affected consumers should stop using the product. Read more at govinfonow.com/recall/17592-goji-powder-recall-fungicide-carbendazim-hazard.
“Goji Powder Recall: Fungicide Carbendazim Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17592-goji-powder-recall-fungicide-carbendazim-hazard. Based on FDA recall #F-1397-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1397-2019%22&limit=1).
The FDA announced on April 8, 2019, that Xi'an Yuens Biological Technology Co., Ltd. voluntarily recalled Goji Powder due to the presence of fungicide carbendazim. The recall affects products distributed in California, Ohio, Texas, Florida, China, Indonesia, Korea, and Australia.
How to tell if you have it
Brand: Xi'an Yuens Biological Technology
Product: Goji Powder (aka Wolfberry Powder)
Lot codes: C17102301, C17121801
Quantity: 10310 kg
The hazard
The product contains the fungicide carbendazim. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show other recent recalls of similar products include Mangalm Tops Strawberry Jam Recall (2025-11-04) and SB FOOD Yoyo Gummy Grape Plus Recall (2025-11-21). Wild Coast Brew Tart Chocolaty Tisane Recall occurred on 2026-06-05.
How to tell if you have this one
Check for product codes C17102301 or C17121801 on the Goji Powder packaging. The product is sold under the brand name Xi'an Yuensun Biological Technology.
Brand
Xi'an Yuens: Biological Technology
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Product
Discard any Goji Powder (Wolfberry Powder) with product codes C17102301 or C17121801 immediately.
Where it went and when
Where it was distributed
Distributed in 4 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “U.S. distribution to the following: CA, OH, TX, and FL Foreign distribution to the following: China, Indonesia, Korea, and Australia.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Florida, Ohio, Texas.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-1397-2019 (April 8, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1397-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.