The Recall Desk
ModerateFDA (Food)·F-2264-2014·Announced 2014-08-06

GM Manufacturing Recalls Garcinia Cambogia Supplements for cGMP Violations

GM Manufacturing is recalling 829 units of Garcinia Cambogia dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, which typically involves a reasonable probability of temporary or medically reversible health consequences. The source cites cGMP violations without reporting specific illnesses or injuries, aligning with the Moderate severity criteria for voluntary precautionary recalls or minor labeling/process errors.

Plain-English summary

GM Manufacturing Inc. is voluntarily recalling 829 units of Garcinia Cambogia dietary supplements packaged in 225cc HDPE bottles. The recall is being conducted because the products were found to have significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements.

The affected products have an expiration date of April 2017 (EXP04.2017). The recall is limited to distribution in California (CA).

Consumers who have purchased these products should stop using them and contact GM Manufacturing Inc. for further instructions or a refund, as per standard recall procedures.

The recalled product

Product
Garcinia Cambogia, 225cc HDPE Bottle
Affected units
829

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • EXP04.2017

Distribution

Distributed in 1 state:

Part of a larger recall action

This product is one of 46 recalled by GM Manufacturing Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 46 products in this recall →