Organic Auricularia auricular recall
Recalled by Aloha Medicinals, Inc. · Carson City, NV, United States
Class I — High risk. Reasonable probability of serious harm or death.
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.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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
Quantity: 502 kgs.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot AA091215; Expiration date: 12/08/2018
Where it was sold
FDA's distribution note: No US Distribution. Three customers in Europe - Italy, Germany and Austria.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Aloha Medicinals, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 29, 2016
- In FDA report of
- Jun 1, 2016
- Terminated
- Oct 6, 2016
- FDA recall number
- F-1284-2016 · event 73707
- Official record
- FDA enforcement report search