Severity
Low
LowClass IIITerminated
FDA Food recall · Reported November 29, 2023
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
ActiPharma, Inc. recalled ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, E… - a low-severity action.
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, E… was recalled by ActiPharma, Inc. in November 29, 2023. Reason: FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet fol…. Check the official notice for the remedy. Verify recall #F-0463-2024 with the FDA Food before acting.
The recall
ActiPharma, Inc. issued this low-severity FDA Food recall-FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet fol….
- Low
- severity level
- Class III
- classification
- November 29, 2023
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0463-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0463-2024) was formally reported on November 29, 2023, with the manufacturer initiating the action on September 28, 2023. It is classified under Low severity (Class III), with a current status of Terminated. ActiPharma, Inc. is listed as the recalling firm, operating out of Guaynabo, PR. Federal records list the affected scope as 607 bottles of 100 tablets each.
The documented reason for this recall is: FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim. Distribution data in the federal record shows the product reached: Domestic distribution, in Puerto Rico.. 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, 6 from FDA Food - 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.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
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.
Affected scope
607 bottles of 100 tablets each
Related Recalls
6
6 from same agency
Product description
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Reason for recall
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-0463-2024 |
| Date reported | November 29, 2023 |
| Date initiated | September 28, 2023 |
| Recalling firm | ActiPharma, Inc. |
| Firm location | Guaynabo, PR |
| Affected scope | 607 bottles of 100 tablets each |
| Distribution | Domestic distribution, in Puerto Rico. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0463-2024) 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? ▼
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.. Recalled by ActiPharma, Inc.. Units affected: 607 bottles of 100 tablets each.
Why was this product recalled? ▼
FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to the label claim.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 29, 2023. Severity: Low. Recall number: F-0463-2024.
Where was the recalled product distributed? ▼
Distribution: Domestic distribution, in Puerto Rico..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0463-2024) 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.
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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
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 November 29, 2023. 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.