Triceutical Inc. Recalls Placenta Dietary Supplements for Manufacturing Violations
Triceutical Inc. is recalling Placenta dietary supplements because they were not produced under good manufacturing practices. The recall covers 227 bottles distributed in Florida, New York, Pennsylvania, and China.
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 recall is classified as FDA Class III, which the rubric defines as unlikely to cause adverse health consequences, typically corresponding to a score of 1 or 2. The hazard is a manufacturing practice violation without reported illness.
Plain-English summary
Triceutical Inc. has initiated a recall of Placenta dietary supplements. The recall was issued because the products were not manufactured in accordance with good manufacturing practices (GMP). The affected product consists of 227 bottles of Placenta, covering all lot numbers and expiration dates.
The recalled products were distributed domestically in Florida, New York, and Pennsylvania, as well as internationally in China. The recall is classified as Class III by the U.S. Food and Drug Administration, indicating that use of or exposure to the violative product is not likely to cause adverse health consequences.
Consumers who have purchased these products should stop using them and contact the recalling firm for further instructions or a refund. No specific illnesses or injuries have been reported in connection with this recall.
The recalled product
- Product
- Placenta
- Manufacturer
- Triceutical Inc./Zhang
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 227
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.
See all 21 products in this recall →Related recalls
Same manufacturer · Triceutical Inc./Zhang
See all →- LowTriceutical Recalls Hyaluronic Acid Supplements Due to Manufacturing Deficiencies
FDA (Food) · 2016-10-26
- LowTriceutical Recalls Premium Protein III Supplement for Manufacturing Deficiencies
FDA (Food) · 2016-10-26
- ModerateTriceutical Recalls Rishi Mushroom Spore Supplements for Manufacturing Violations
FDA (Food) · 2016-10-26
- ModerateTriceutical Recalls Lecithin Reishi Complex Soft Gels for Manufacturing Issues
FDA (Food) · 2016-10-26
- LowTriceutical Inc. Recalls CardioAdvance Dietary Supplements for Manufacturing Violations
FDA (Food) · 2016-10-26
Same hazard · gmp violation
See all →- HighVista Meibo Tears eye drops recalled over sterility assurance failure
FDA (Drugs) · 2026-03-04
- HighBio Glo fluorescein strips 300-count recalled over sterility assurance failure
FDA (Drugs) · 2026-03-04
- HighBioGlo fluorescein ophthalmic strips recalled over sterility assurance failure
FDA (Drugs) · 2026-03-04
- HighVista Tears lubricant eye drops recalled over sterility assurance failure
FDA (Drugs) · 2026-03-04
- ModerateRapidol Arnica Gel topical homeopathic medicine recalled for manufacturing violations
FDA (Drugs) · 2025-04-30