GM Manufacturing recalls Tendon & Muscle Plus bottles due to cGMP regulatory violations in dietary supplements. Consumers should check product labels for the 509EXP05.2:2015 expiration date.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling Tendon & Muscle Plus bottles because they were made without following food safety regulations. This could mean the supplements might not be safe or could cause health issues.
The supplements were made without following food safety regulations. This could lead to unsafe products that might cause health problems. The exact risk level isn't clearly stated in the recall notice.
People who bought Tendon & Muscle Plus bottles with the expiration date 509EXP05.2.2015 are affected. Those using dietary supplements for health reasons may be at risk.
Check the product label for the expiration date 509EXP05.2.2015. The product name is Tendon & Muscle Plus bottles.
Look for the expiration date 509EXP05.2.2015 on the bottle label.
GM Manufacturing is recalling these supplements due to significant violations of cGMP regulations for dietary supplements.
The recall notice does not specify a remedy, so check the product label for the expiration date 509EXP05.2.2015.
The recall notice does not describe a specific hazard mechanism that could cause serious injury.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2283-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2283-2014 from GM Manufacturing. 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.
