GM Manufacturing recalls Double Mojo dietary supplements with lot numbers LOT08172013 (expiring Dec 2016) due to significant cGMP regulatory violations.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling Double Mojo dietary supplements because they violated cGMP regulations. This recall affects consumers who bought these supplements with the lot number LOT081:72013, which expired in December 2016.
The supplements were made in violation of current Good Manufacturing Practices (cGMP) regulations. This means the product may not be safe or effective as intended, but the specific health risks are not detailed in the recall notice.
Consumers who purchased Double Mojo dietary supplements with lot number LOT08172013 (expiring Dec 2016) are affected. Those who used these supplements after the expiration date are at higher risk.
Check the lot number on the product label, which should be LOT08172013. The product expires in December 2016. This recall applies to dietary supplements sold by GM Manufacturing.
Look for the lot number LOT08172013 on the product label to confirm if it is affected.
GM Manufacturing is recalling these dietary 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 lot number LOT08172013 and contact GM Manufacturing for further instructions.
The recall notice does not describe specific health risks, so the danger level is unknown.
We’ve drafted a message you can send GM Manufacturing to request your refund or repair — edit it as you like.
Subject: Recall F-2254-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2254-2014 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.
