OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Summary
The FDA issued a Class III for OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with bla by Optiwize Inc.. Reason: The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results, manganes.
Details
Source
Food Recall
External ID
H-0442-2026
Action Date
2026-02-11
Status
Completed
Category
food
Product Description
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Lot/Code Info: OHB25230
Quantity Affected: 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.
Distribution
Nationwide via Amazon distribution
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-23
Company
Buda, TX
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Optiwize Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Optiwize Inc. have FDA actions?
This is the only FDA action we have on record for Optiwize Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0442-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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