FDA recall record
Organic Auricularia auricular (Dried Mushroom Powder (Jelly Ear Mushroom). 60 kg 4 mil polyethylene bags inside plastic polyethylene black drum. Certified Organic by QAI - M...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of October 6, 2016. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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
Code information listed by FDA
Lot AA091215; Expiration date: 12/08/2018
Distribution and firm information
Recalling firm listed by FDA: Aloha Medicinals, Inc.
Firm location listed by FDA: Carson City, NV, United States
Distribution reported by FDA: No US Distribution. Three customers in Europe - Italy, Germany and Austria.
Product quantity listed by FDA: 502 kgs.
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.