The Recall Desk
ModerateFDA (Food)·F-2260-2014·Announced 2014-08-06

GM Manufacturing Recalls Chanca Piedra Dietary Supplements for cGMP Violations

GM Manufacturing is recalling 378 bottles of Chanca Piedra 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 a Moderate severity rating for regulatory non-compliance.

Plain-English summary

GM Manufacturing Inc. is voluntarily recalling 378 units of Chanca Piedra dietary supplements, packaged in 225cc HDPE bottles. The product is identified by the expiration date EXP10.2016.

The recall was initiated because the dietary supplements were found to have significant violations of the current Good Manufacturing Practice (cGMP) regulations. These regulations are designed to ensure that products are consistently produced and controlled according to quality standards.

The affected product was distributed in California (CA). Consumers who possess this product should stop using it and contact the recalling firm for further instructions or a refund.

The recalled product

Product
Chanca Piedra, 225cc HDPE Bottles
Affected units
378

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)

  • EXP10.2016

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 →