RecallHawk
Class III Recall

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

Optiwize Inc.

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

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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