The Recall Desk
ModerateFDA (Food)·F-2277-2014·Announced 2014-08-06

GM Manufacturing Recalls Kidney&Chi Plus Dietary Supplements for cGMP Violations

GM Manufacturing is recalling Kidney&Chi Plus 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 situation where use of, or exposure to, a violative product may cause temporary or medically reversible adverse 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 recalling Kidney&Chi Plus dietary supplements. 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 are identified by the codes 724EXP08.2015 and EXP12.2015. A total of 674 units were distributed in California (CA). The source text does not specify specific health hazards, illnesses, or injuries associated with these violations.

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
Kidney&Chi Plus, Bottles
Affected units
674

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)

  • 724EXP08.2015 EXP12.2015

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 →