Recall record at a glance
| Official record | F-0738-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | GOLDEN MEDAL MUSHROOM Inc. |
| Report date | Feb 23, 2022 |
| Recall initiation date | Feb 4, 2022 |
| Quantity | 36 cartons |
| Location | Commerce, CA, United States |
Official product description
Enoki Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce packages, UPC 6 953150 100684. Product sent to distributor is packaged in a brown cardboard master case. The product name "ENOKI MUSHROOM" and other information in Chinese are printed in green color. The code "300511" is printed in blue color.
Why the product was recalled
Michigan Department of Agriculture and Rural Development sampled product and Listeria monocytogenes was detected.
Distribution information
Distributed in IL.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.