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Class I: serious health riskTerminated

Aloha Medicinals Organic Auricularia auricular Recall

Organic Auricularia auricular (Dried Mushroom Powder (Jelly Ear Mushroom)

Aloha Medicinals, Inc. · Carson City, NV

Risk level
Class I
Reported by FDA
Jun 1, 2016
Recall ID
F-1284-2016
Check your lot numberHow we source this data

Summary

Aloha Medicinals recalled Organic Auricularia auricular starting Mar 29, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-1284-2016 on Jun 1, 2016. Reason: One retained sample of Auricularia auricular tested positive for E-Coli. Product was tested after firm received reports of stomach issues from wholesale customer. Status: Terminated.

Why it was recalled

One retained sample of Auricularia auricular tested positive for E-Coli. Product was tested after firm received reports of stomach issues from wholesale customer.

Product description

Organic Auricularia auricular (Dried Mushroom Powder (Jelly Ear Mushroom). 60 kg 4 mil polyethylene bags inside plastic polyethylene black drum. Certified Organic by QAI - Made in USA. Aloha Medicinals Inc. 2300 Arrowhead Drive Carson City, NV 89706

Lot numbers, UPCs & expiration codes

Lot AA091215; Expiration date: 12/08/2018

Where it was sold

No US Distribution. Three customers in Europe - Italy, Germany and Austria.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1284-2016
Classification
Class I
Status
Terminated
Recall initiated
Mar 29, 2016
FDA report date
Jun 1, 2016
Quantity
502 kgs.
Recall type
Voluntary: Firm initiated
Recalling firm
Aloha Medicinals, Inc.

Original FDA data

Every field from FDA enforcement report F-1284-2016, exactly as published.

Show all FDA fields
City
Carson City
State
NV
Status
Terminated
Country
United States
Event ID
73707
Address
2300 Arrowhead Dr
Code information
Lot AA091215; Expiration date: 12/08/2018
Postal code
89706-0405
Report date
Jun 1, 2016
Product type
Food
Recall number
F-1284-2016
Classification
Class I
Recalling firm
Aloha Medicinals, Inc.
Product quantity
502 kgs.
Termination date
Oct 6, 2016
Reason for recall
One retained sample of Auricularia auricular tested positive for E-Coli. Product was tested after firm received reports of stomach issues from wholesale customer.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Organic Auricularia auricular (Dried Mushroom Powder (Jelly Ear Mushroom). 60 kg 4 mil polyethylene bags inside plastic polyethylene black drum. Certified Organic by QAI - Made in USA. Aloha Medicinals Inc. 2300 Arrowhead Drive Carson City, NV 89706
Distribution pattern
No US Distribution. Three customers in Europe - Italy, Germany and Austria.
Recall initiation date
Mar 29, 2016
Initial firm notification
Letter
Center classification date
May 20, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1284-2016, published Jun 1, 2016. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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