PlainRecalls
LowClass IIICompleted

FDA Food recall · Reported February 11, 2026

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

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 quant…

Recall #
H-0442-2026
Affected scope
78 units
Initiated
September 23, 2025
Verify with FDA Food →
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Optiwize Inc. recalled OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid. - a low-severity action.

OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid. was recalled by Optiwize Inc. in February 11, 2026. Reason: The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not ali…. Check the official notice for the remedy. Verify recall #H-0442-2026 with the FDA Food before acting.

The recall

Optiwize Inc. issued this low-severity FDA Food recall-The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not ali….

Low
severity level
78 units
affected scope
Class III
classification
February 11, 2026
reported

Sourced from official FDA Food enforcement records. Verify recall #H-0442-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #H-0442-2026) was formally reported on February 11, 2026, with the manufacturer initiating the action on September 23, 2025. It is classified under Low severity (Class III), with a current status of Completed. Optiwize Inc. is listed as the recalling firm, operating out of Buda, TX. Federal records list the affected scope as 78 units.

The documented reason for this recall is: 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 data in the federal record shows the product reached: Nationwide via Amazon distribution. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Children & Baby Products recalls over time

Where this recall sits in its category - 3,731 children & baby products recalls on record

0100200300400500600 20052008201120142017202020232026 146
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Low

Affected scope

78 units

Related Recalls

6

0 from same agency

Product description

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

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.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Completed
Recall number H-0442-2026
Date reported February 11, 2026
Date initiated September 23, 2025
Recalling firm Optiwize Inc.
Firm location Buda, TX
Affected scope 78 units
Distribution Nationwide via Amazon distribution

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

78 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (H-0442-2026) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid.. Recalled by Optiwize Inc.. Units affected: 78 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Food on February 11, 2026. Severity: Low. Recall number: H-0442-2026.
Where was the recalled product distributed?
Distribution: Nationwide via Amazon distribution.
How do I check if my product is affected by a recall?
Check the product description and recall number (H-0442-2026) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

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Browse all Children & Baby Products recalls →

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported February 11, 2026. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.