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Class IIITerminated in FDA datasetRecall initiated Aug 21, 2019

FungusAmongUs Shiitake Organic Mushrooms are dried mushrooms. Packaged in a clear cellophane…

Recalling firm: Seattle Gourmet Foods Inc.

Why it 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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 17, 2019.

Check your package

Compare the exact product and package details with the label you have.

ProductFungusAmongUs 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 ***".
Package size1 ounce
UPC719870600233

FDA code information

Code is found on the package with a sticker: 11498 Best By 050121 21418 Best By 050121

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Full FDA record and distribution details

Original 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 ***".

Extracted codes and context

TypeCode / valueContext
UPC719870600233dried 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

Original FDA recall reason

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.

Recall details

Recall number
F-2151-2019
Event ID
83611
FDA status
Terminated
Initiated
Aug 21, 2019
Reported
Sep 18, 2019
Classified
Sep 11, 2019
Terminated
Oct 17, 2019
Quantity
3328/1 oz. packages
Location
Tukwila, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

nationwide

FDA source record · F-2151-2019

Data updated September 16, 2026. View official FDA data ↗

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