GM Manufacturing recalls Bone & Joint Plus bottles for significant cGMP violations in dietary supplements. Consumers should check product labels for 819EXP08.2:2015.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling Bone & Joint Plus bottles after finding significant violations of cGMP regulations for dietary supplements. This recall affects products with the label 819EXP08.2015.
The recall is due to significant violations of current Good Manufacturing Practices (cGMP) regulations for dietary supplements. These violations could lead to unsafe product quality, but the specific hazard mechanism isn't detailed in the notice.
Dietary supplement users who purchased Bone & Joint Plus bottles with the label 819EXP08.2015 are affected. People using these products may be at risk due to regulatory violations.
Check the product label for the code 819EXP08.2015. This is the specific batch number for the recalled Bone & Joint Plus bottles.
Look for the label code 819EXP08.2015 on the bottle to confirm if it's recalled.
GM Manufacturing is recalling Bone & Joint Plus bottles due to significant violations of cGMP regulations for dietary supplements.
Check the product label for the code 819EXP08.2015. If it matches, you should stop using it and contact GM Manufacturing for further instructions.
The recall is due to regulatory violations, but the specific hazard mechanism isn't detailed in the notice. The official notice does not mention injury risks.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2281-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2281-2014 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.
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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.
