OptiWize Health OptiWize Collagen Plus recall
Recalled by Optiwize Inc. · Buda, TX, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
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.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Quantity: 78 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
OHB25230
Where it was sold
Nationwide.
FDA's distribution note: Nationwide via Amazon distribution
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Optiwize Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 23, 2025
- In FDA report of
- Feb 11, 2026
- Terminated
- Sep 21, 2026
- FDA recall number
- H-0442-2026 · event 98263
- Official record
- FDA enforcement report search