Good Herbs Inc. recalls Respiratory Plus 1oz bottles made on or after Oct 17, 2013 for not meeting Good Manufacturing Practices. Consumers should check product date and contact for details.
Products not manufactured under GMP's
Good Herbs Inc. is recalling Respiratory Plus 1oz bottles produced on or after October 17, 2013 because they were not made under Good Manufacturing Practices. This could mean the product isn't safe or reliable for use.
Products not made under Good Manufacturing Practices (GMPs) may not meet safety or quality standards. This could lead to inconsistent product performance or potential health risks, though the specific danger isn't detailed in the recall.
People who bought Respiratory Plus 1oz bottles from Good Herbs Inc. in the U.S. after October 17, 2013. Those with respiratory issues might be at slightly higher risk if the product isn't properly manufactured.
Check for the product name 'Respiratory Plus', 1oz bottle, and the manufacturing date on or after October 17, 2013. The product was sold by Good Herbs Inc. at 550 Oliver Dr Troy, MI 48084.
Look for the manufacturing date on the bottle, which should be on or after October 17, 2013.
Reach out to Good Herbs Inc. for further instructions on what to do with the recalled product.
The recall states the products were not manufactured under Good Manufacturing Practices, but the specific danger isn't detailed in the notice.
Check for the product name 'Respiratory Plus', 1oz bottle, and the manufacturing date on or after October 17, 2013.
Contact Good Herbs Inc. for instructions on what to do with the recalled product.
We’ve drafted a message you can send Good Herbs to request your refund or repair — edit it as you like.
Subject: Recall F-0396-2015 — Good Herbs Good Herbs Hello, I own a Good Herbs that is covered by recall F-0396-2015 from Good Herbs. 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.
