FDA recall record
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of September 21, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Code information listed by FDA
OHB25230
Distribution and firm information
Recalling firm listed by FDA: Optiwize Inc.
Firm location listed by FDA: Buda, TX, United States
Distribution reported by FDA: Nationwide via Amazon distribution
Product quantity listed by FDA: 78 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.