OptiWize Health OptiWize Collagen Plus 320 count bottle
Recalled by Optiwize Inc.
Food recall
Optiwize Inc.
Class III — least serious
Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
Optiwize Inc. has recalled OptiWize Health OptiWize Collagen Plus 320 count bottle, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 11, 2026 and was initiated on September 23, 2025. It is classified as a Class III recall, which means using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers OptiWize Health OptiWize Collagen Plus 320 count bottle, with approximately 78 units affected. The company behind the recall is Optiwize Inc., based in Buda, TX. The FDA describes the product as: “OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.”
Why was OptiWize Health OptiWize Collagen Plus 320 count bottle recalled?
According to the FDA, the stated reason for the recall is: “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.”
What should you do?
If you think you may have bought OptiWize Health OptiWize Collagen Plus 320 count bottle, compare it against the product description and identifying codes (OHB25230) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Optiwize Inc. or your local health authority.
About this recall
This recall was distributed in TX. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Completed
- Date reported
- February 11, 2026
- Recall started
- September 23, 2025
- Distributed in
- TX
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was OptiWize Health OptiWize Collagen Plus 320 count bottle recalled?+
According to the FDA: The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities…
How serious is this recall?+
Class III — least serious. Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
What should I do if I have OptiWize Health OptiWize Collagen Plus 320 count bottle?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0442-2026. Information last synced from the FDA on July 5, 2026.