Recall record at a glance
| Official record | F-2151-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Seattle Gourmet Foods Inc. |
| Report date | Sep 18, 2019 |
| Recall initiation date | Aug 21, 2019 |
| Quantity | 3328/1 oz. packages |
| Location | Tukwila, WA, United States |
Official product description
FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a clear cellophane bag, net Weight 1 ounce. UPC 7 19870 60023 3 for individual 1 ounce bags UPC 50719870600016 for Master caddy that holds 8 packages of 1 ounce bags The label is read in parts: "***Organically Grown Shiitake Mushrooms ***FUNGUSAMONGUS***Product of China ***".
Why the product was recalled
FungusAmongUs Shiitake Organic Mushrooms are recalled due to undeclared Sulfites. the Florida Department of Agriculture and Consumer Services tested and found 0.33 mg Sulfites per serving.
Distribution information
nationwide
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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.