Triceutical Inc. recalls RISHI Mushroom Spore dietary supplements due to lack of good manufacturing practices. Consumers should check product lot numbers for affected items.
Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.
Triceutical Inc. has recalled all RISHI Mushroom Sp: 60-count supplements sold in boxes of 24 due to lack of good manufacturing practices. This recall affects consumers who may have purchased these supplements and poses a risk from potential contamination.
The recall is due to lack of good manufacturing practices, which could lead to potential contamination of the supplements. This means the product may not meet safety standards and could pose health risks to consumers.
Anyone who purchased RISHI Mushroom Spore dietary supplements from Triceutical Inc. or Zhang. Consumers who have the product are most at risk due to potential contamination.
Check for the product name 'RISHI MUSHROOM SPORE', 60 count, 24 per box. Look for lot number 1222412 on the packaging.
Look for the product name 'RISHI MUSHROOM SPORE', 60 count, 24 per box, and lot number 1222412 on the packaging.
The recall is due to lack of good manufacturing practices, which could lead to potential contamination of the supplements.
Check for the product name 'RISHI MUSHROOM SPORE', 60 count, 24 per box, and lot number 1222412 on the packaging.
The recall does not specify a remedy, so consumers should check with Triceutical Inc. for further instructions.
We’ve drafted a message you can send Triceutical to request your refund or repair — edit it as you like.
Subject: Recall F-0092-2017 — Triceutical Triceutical Hello, I own a Triceutical that is covered by recall F-0092-2017 from Triceutical. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.