Severity
Moderate
ModerateActive
CPSC recall · Reported June 22, 2023
Nationwide Pharmaceutical Recalls Iron Dietary Supplements Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products i…
Prodigy Innovation LLC, of Princeton, New Jersey recalled This recall involves Ferrous Sulfate Enteric-Coated Tablets dietary supplements containin… - a moderate-severity action.
Nationwide Pharmaceutical Recalls Iron Dietary Supplements Due to Failure to Meet Child R… was recalled by Prodigy Innovation LLC, of Princeton, New Jersey in June 22, 2023. Reason: The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the P…. Remedy: Consumers should immediately store the recalled dietary supplements in a safe location ou…. Verify recall #23227 with the CPSC before acting.
The recall
Prodigy Innovation LLC, of Princeton, New Jersey issued this moderate-severity CPSC recall-The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the P….
- Moderate
- severity level
- June 22, 2023
- reported
Sourced from official CPSC enforcement records. Verify recall #23227 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This CPSC action (record #23227) was formally reported on June 22, 2023. It is classified under Moderate severity, with a current status of Active. Prodigy Innovation LLC, of Princeton, New Jersey is listed as the recalling firm. Federal records list the affected scope as About 4,000.
The documented reason for this recall is: The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child-resistant, posing a risk of … Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately store the recalled dietary supplements in a safe location out of reach and sight of children and contact Nationwide Pharmaceutical for information on how to dispose of th… - consumers holding this product should act on that instruction rather than relying on general guidance.
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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,287 drugs & medications 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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
About 4,000
Related Recalls
6
0 from same agency
Product description
This recall involves Ferrous Sulfate Enteric-Coated Tablets dietary supplements containing 324 mg of ferrous sulfate (iron) in bottles of 100 tablets. "Nationwide Pharmaceutical" and its logo are printed on the top left of the bottle's label panel. The recalled bottles include lot numbers M0786, M0816, M0817 and M0818, which are printed on the bottom of the bottle.
Reason for recall
The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.
Remedy, what to do
Consumers should immediately store the recalled dietary supplements in a safe location out of reach and sight of children and contact Nationwide Pharmaceutical for information on how to dispose of the product. Consumers can also return the product to the place of purchase to receive a refund of the purchase price.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 23227 |
| Date reported | June 22, 2023 |
| Date initiated | June 22, 2023 |
| Recalling firm | Prodigy Innovation LLC, of Princeton, New Jersey |
| Affected scope | About 4,000 |
| Distribution | Not disclosed |
| Official source | CPSC notice → |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
What to do with this recall
Consumers should immediately store the recalled dietary supplements in a safe location out of reach and sight of children and con…
- Check the recall number (23227) and product description against the item you own. Search the archive
- Confirm the current status and remedy on the official CPSC notice before acting. CPSC notice
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official CPSC 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? ▼
This recall involves Ferrous Sulfate Enteric-Coated Tablets dietary supplements containing 324 mg of ferrous sulfate (iron) in bottles of 100 tablets. "Nationwide Pharmaceutical" and its logo are printed on the top left of the bottle's label panel. The recalled bottles include lot numbers M0786, M0816, M0817 and M0818, which are printed on the bottom of the bottle.. Recalled by Prodigy Innovation LLC, of Princeton, New Jersey. Units affected: About 4,000.
Why was this product recalled? ▼
The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.
What should consumers do? ▼
Consumers should immediately store the recalled dietary supplements in a safe location out of reach and sight of children and contact Nationwide Pharmaceutical for information on how to dispose of the product. Consumers can also return the product to the place of purchase to receive a refund of the purchase price.
Which agency issued this recall? ▼
This recall was issued by the CPSC on June 22, 2023. Severity: Moderate. Recall number: 23227.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (23227) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product? ▼
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.
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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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: CPSC, reported June 22, 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.