GM Manufacturing recalls Garcinia Cambogia dietary supplements due to cGMP regulatory violations. Consumers should check product labels for 225cc HDPE bottles with expiration date 04.2017.
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
GM Manufacturing is recalling Garcinia Camb: 225cc HDPE bottles sold with expiration date 04.2017 due to significant violations of cGMP regulations for dietary supplements. This recall addresses potential quality and safety issues in the product.
The product was found to have significant violations of current Good Manufacturing Practices (cGMP) regulations for dietary supplements. These violations could lead to quality and safety issues in the product, though the specific hazard mechanism isn't detailed in the recall notice.
Dietary supplement users who purchased the Garcinia Cambogia 225cc HDPE bottle with expiration date 04.2017 are affected. Those who have the product are at risk due to regulatory violations.
Check for Garcinia Cambogia supplements in 225cc HDPE bottles with expiration date 04.2017. The product was sold by GM Manufacturing Inc.
Look for the product name 'Garcinia Cambogia', 225cc HDPE bottle, and expiration date 04.2017 on the label.
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 or action for consumers.
The recall notice does not describe a specific hazard mechanism or risk of 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-2264-2014 — GM Manufacturing GM Manufacturing Hello, I own a GM Manufacturing that is covered by recall F-2264-2014 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.
