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Class III: unlikely to cause harmTerminated

OptiWize Health OptiWize Collagen Plus 320 Recall

OptiWize Health OptiWize Collagen Plus 320 count bottle

Optiwize Inc. · Buda, TX

Risk level
Class III
Reported by FDA
Feb 11, 2026
Recall ID
H-0442-2026
Check your lot numberHow we source this data

Summary

Optiwize recalled OptiWize Health OptiWize Collagen Plus 320 starting Sep 23, 2025. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report H-0442-2026 on Feb 11, 2026. 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. Status: Terminated.

Why it was recalled

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.

Lot numbers, UPCs & expiration codes

OHB25230

Where it was sold

Nationwide via Amazon distribution

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
H-0442-2026
Classification
Class III
Status
Terminated
Recall initiated
Sep 23, 2025
FDA report date
Feb 11, 2026
Quantity
78 units
Recall type
Voluntary: Firm initiated
Recalling firm
Optiwize Inc.

Original FDA data

Every field from FDA enforcement report H-0442-2026, exactly as published.

Show all FDA fields
City
Buda
State
TX
Status
Terminated
Country
United States
Event ID
98263
Address
1220 Satterwhite Rd Ste 902
Code information
OHB25230
Postal code
78610-3984
Report date
Feb 11, 2026
Product type
Food
Recall number
H-0442-2026
Classification
Class III
Recalling firm
Optiwize Inc.
Product quantity
78 units
Termination date
Sep 21, 2026
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.
Distribution pattern
Nationwide via Amazon distribution
Recall initiation date
Sep 23, 2025
Initial firm notification
E-Mail
Center classification date
Feb 2, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report H-0442-2026, published Feb 11, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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