Food recall
Optiwize Inc. recall: OptiWize Health OptiWize Collagen Plus 320 count bottle
Optiwize Inc., of Buda, TX, recalled OptiWize Health OptiWize Collagen Plus 320 count bottle. The FDA's reason: “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.” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on September 23, 2025, and the FDA first listed it in its Enforcement Report of February 11, 2026. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class III
It is unlikely to cause harm
Why
Labeling, packaging or manufacturing problems
Status
Terminated
Closed September 21, 2026
The recall
- Company
- Optiwize Inc. (Buda, TX)
- Reason, in FDA's words
- “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.”
- Where it was sold
- Nationwide via Amazon distribution
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 98263
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
H-0442-2026 Class III
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Codes: OHB25230
Quantity: 78 units
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of February 11, 2026.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.