← FDA ENFORCEMENT
H-0442-2026Class III

Optiwize Inc.

Recalling firm
Optiwize Inc.
Product type
Food / supplement / cosmetic
Status
Completed
Report date
2026-02-11
Distribution
Nationwide via Amazon distribution
Firm state
TX
Product quantity
78 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
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.

Product description

OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.

Code / lot info

OHB25230

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.