Optiwize Inc. Recalls OptiWize Health OptiWize Collagen Plus 320 count bottle
This is a Class III recall. This product is unlikely to cause adverse health reactions but violates FDA regulations.
Optiwize Inc. Recalls OptiWize Health OptiWize Collagen Plus 320 count bottle
Optiwize Inc. · Class III — Regulatory

Product Description
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Reason for Recall
The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results, manganese level was below label quantity.
FDA Classification
Class III — Regulatory
A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences.
Distribution
Nationwide via Amazon distribution
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
The FDA has classified this as a Class III recall — the lowest severity level — for a food product recalled by Optiwize Inc. on September 23, 2025. The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results, manganese level was below label quantity. This recall covers 78 units, distributed nationwide. Class III recalls typically involve products unlikely to cause health problems but that violate FDA manufacturing or labeling regulations.
Sources: FDA openFDA Enforcement Database
This recall appears in: Other Injury Hazards.