Triceutical Inc. Recalls CardioAdvance Dietary Supplements for Manufacturing Violations
Triceutical Inc. is recalling all CardioAdvance dietary supplements because the products were not manufactured according to good manufacturing practices.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The FDA classified this recall as Class III, which indicates that the product is unlikely to cause adverse health consequences. The recall is due to a lack of good manufacturing practices, which is a documentation and process issue rather than a direct safety hazard like contamination or mislabeling.
Plain-English summary
Triceutical Inc. has initiated a recall of all CardioAdvance dietary supplements. The recall was issued because the products were not manufactured in accordance with good manufacturing practices (GMP).
The recall includes 528 bottles of CardioAdvance. The affected products include all lot numbers and all expiration dates. Distribution of the recalled products occurred in Florida, New York, and Pennsylvania, as well as in China.
Consumers who have purchased CardioAdvance should stop using the product and contact Triceutical Inc. for further instructions or a refund.
The recalled product
- Product
- CardioAdvance
- Manufacturer
- Triceutical Inc./Zhang
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 528
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 (2)
- all lot numbers
- all expiration dates
Distribution
Part of a larger recall action
This product is one of 21 recalled by Triceutical Inc./Zhang 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.
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