CardioAdvance (Triceutical Inc.) – Manufacturing practices (2014)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
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
CardioAdvance
Brand
Triceutical Inc./Zhang
Lot Codes / Batch Numbers
all lot numbers, all expiration dates
Products Sold
all lot numbers, all expiration dates
Triceutical Inc./Zhang is recalling CardioAdvance due to Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.. 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
Triceutical Inc. has recalled all dietary supplements due to lack of good manufacturing practices.
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
FL, NY, PA
Page updated: Jan 6, 2026