Aloha Medicinals recalls organic dried jelly ear mushroom powder after one sample tested positive for E. coli. Product sold in 60kg bags with expiration date 12/08/2018.
One retained sample of Auricularia auricular tested positive for E-Coli. Product was tested after firm received reports of stomach issues from wholesale customer.
Aloha Medicinals is recalling organic dried jelly ear mushroom powder after one sample tested positive for E. coli. This recall follows reports of stomach issues from a wholesale customer. Consumers should stop using the product if they have it.
One sample of the dried mushroom powder tested positive for E. coli bacteria. The product was tested after reports of stomach issues from a wholesale customer. This indicates a potential risk of foodborne illness.
Anyone who purchased the organic dried jelly ear mushroom powder from Aloha Medicinals. People who have the product with lot number AA091215 and expiration date 12/08/2018 are most at risk.
Check for the product name 'Organic Auricularia auricular (Dried Mushroom Powder)' in 60kg bags with a black polyethylene drum. Look for lot number AA091215 and expiration date 12/08/2018.
If you have the recalled product with lot number AA091215 and expiration date 12/08/2018, stop using it immediately.
The recall was initiated after one sample tested positive for E. coli, but the product is not confirmed safe for consumption.
Stop using the product immediately if you have it with lot number AA091215 and expiration date 12/08/2018.
Check for the lot number AA091215 and expiration date 12/08/2018 on the product packaging.
We’ve drafted a message you can send Aloha Medicinals to request your refund or repair — edit it as you like.
Subject: Recall F-1284-2016 — Aloha Medicinals Aloha Medicinals Hello, I own a Aloha Medicinals that is covered by recall F-1284-2016 from Aloha Medicinals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
