Recall record at a glance
| Official record | F-1634-2012 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | LA Link Corporation |
| Report date | Jun 27, 2012 |
| Recall initiation date | May 22, 2012 |
| Quantity | 27,648 jars |
| Location | Cerritos, CA, United States |
Official product description
Shiitake-Ya brand Dried Shiitake mushroom slices, 6 oz plastic jars, UPC 7 1452 22183 9. Product labeling reads in part: " Shiitake-Ya gourmet Shiitake SLICES***Antioxidants Amino Acids Omega 3+6***Immune-Boosting*** NET WEIGHT. 6 oz (170 g)***Natural Enzymes Fiber (80% Chitin) Iron Kojic Acid
Why the product was recalled
Shiitake-Ya Gourmet Shiitake slices are being recalled because FDA test analysis showed presence of pesticide and polycyclic aromatic hydrocarbon residues: 0.208 ppm carbendazim, 0.072 ppm Fluoranthene and 0.092 ppm Pyrene. There are no tolerances for any of these pesticide residues.
Distribution information
Distributed to retail in the following states: HI, NV, CA
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: 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.