Shiitake-ya Brand Dried Shiitake Mushroom Slices, 6 OZ Plastic Jars
What you need to know
Class III
What happened
Shiitake-Ya Gourmet Shiitake slices are being recalled because FDA test analysis showed presence of pesticide and polycyclic aromatic hydrocarbon residues: 0.208 ppm…
Health risk
The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
Action required
Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.
Recall closed · classified by the FDAIN, HI, NV, CAMore supplements
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Distributed to retail in the following states: HI, NV, CA
United States
Quantity affected
27, 648 jars
Recall initiation
FDA report date: June 27, 2012
FDA recall number
F-1634-2012
Beyond the headline
The recall, in context
La Link Corporation initiated this supplements recall on May 22, 2012. The FDA enforcement report states: 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. The FDA report lists distribution as: Distributed to retail in the following states: HI, NV, CA.
The FDA enforcement report describes the reason as: 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.
Shiitake-ya Brand Dried Shiitake Mushroom Slices, 6 OZ Plastic Jars was made or distributed by La Link Corporation in Cerritos, CA, United States. This page reflects FDA report F-1634-2012, dated June 27, 2012.
Why this is a Class III recall
Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
FDA definition
The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.
What to do now
1
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the UPC and lot code against the table above.
3
Return or discard
Contact the retailer or recalling firm about a refund, and dispose of the product safely.
Consumer safety guide
Product safety recall
Symptoms to watch for
The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.
Higher-risk groups
Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.
What to do now
1Stop using or eating the product and keep it away from children and pets.
2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
3Seek medical advice if anyone develops severe or worrying symptoms after exposure.
Read the official source record for the specific hazard and instructions.
This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.
Frequently asked
Questions about this recall
4 answers
What is the Shiitake-ya Brand Dried Shiitake Mushroom Slices, 6 OZ Plastic Jars recall?
La Link Corporation recalled Shiitake-ya Brand Dried Shiitake Mushroom Slices, 6 OZ Plastic Jars in an FDA Class III enforcement action reported as F-1634-2012. Shiitake-Ya Gourmet Shiitake slices are being recalled because FDA test analysis showed presence of pesticide and polycyclic aromatic hydrocarbon residues: 0.208 ppm…
What should I do if I bought this product?
Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.
Is the La Link Corporation recall still active?
The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.
Where can I verify this recall?
This page is normalized from the openFDA enforcement record F-1634-2012. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.
Verify before you act.
VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.