Class IIITerminatedVoluntary: Firm initiated

Optiwize Inc.: food recall H-0442-2026

Optiwize Inc. of Buda, TX recalled OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid. 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 listed it as Class III in its Enforcement Report dated Feb 11, 2026; distribution: nationwide.

Record status as published: Terminated (terminated Sep 21, 2026). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Product quantity
78 units
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.
Codes, lots and dates on the package
OHB25230
Distribution pattern
Nationwide via Amazon distribution
Recalling firm
Optiwize Inc., Buda, TX
Classification
Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
E-Mail

Dates

EventDate
Recall initiated by the firmSep 23, 2025
Classified by the FDAFeb 2, 2026
Published in the Enforcement ReportFeb 11, 2026
TerminatedSep 21, 2026

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0442-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.