Kidney&Chi Plus (GM Manufacturing) – Manufacturing Violations (2014)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Kidney&Chi Plus, Bottles
Brand
GM Manufacturing Inc.
Lot Codes / Batch Numbers
724EXP08.2015 EXP12.2015
Products Sold
724EXP08.2015 EXP12.2015
GM Manufacturing Inc. is recalling Kidney&Chi Plus, Bottles due to GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA
Page updated: Jan 6, 2026