Optiwize Inc. Issues Voluntary Recall for OptiWize Collagen Plus Over Ingredient Discrepancy
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Optiwize Inc. is recalling 78 bottles of OptiWize Collagen Plus sold nationwide via Amazon after testing showed manganese levels were below the amount listed on the label.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 6, 2026 and geographically references United States. Its severity classification of "low" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, supplements.
What Happened
Optiwize Inc. has initiated a voluntary recall of its OptiWize Collagen Plus dietary supplement. The recall was prompted after analytical testing conducted by NSF revealed that the quantity of manganese in the product did not align with the levels stated on the label. Specifically, the manganese levels were found to be below the labeled quantity.
Which Products Are Affected
The recall involves 78 units of the following product:
- Product Name: OptiWize Health OptiWize Collagen Plus
- Packaging: 320-count white bottle with a black lid
- Code Information: OHB25230
- Recall Number: H-0442-2026
These products were distributed nationwide across the United States through Amazon distribution channels.
What You Should Do
Consumers who have purchased the affected bottles of OptiWize Collagen Plus should verify the code information on their packaging. As this is a Class III recall—a category used when a product is unlikely to cause adverse health consequences—the primary issue concerns the accuracy of the nutritional labeling. Consumers seeking further information or potential remedies should contact Optiwize Inc. at their Buda, Texas, headquarters.
Why This Matters
This recall is necessary to ensure that consumers receive the specific nutrient levels promised on the product packaging and to maintain the accuracy of dietary supplement labeling standards.
Source
Information provided by the FDA.
Original source: FDA Official Notice ↗
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