Severity
Moderate
Prodigy Innovation LLC, of Princeton, New Jersey issued this CPSC recall on June 22, 2023. Classified as Moderate severity. Approximately About 4,000 units are affected. The recall was issued because: The recalled dietary supplements contain iron which must be in child-resistant packaging as required by the Poison Prev…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
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 indicate About 4,000 units are affected.
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.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 1 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 3 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Moderate
Units Affected
About 4,000
Related Recalls
6
1 from same agency
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.
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.
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.
| 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 |
| Units affected | About 4,000 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
Learn how the US recall system works and how to protect yourself and your household.
How the US Recall System Works
The three federal agencies, how recalls are initiated, and what happens next.
Understanding Recall Severity Classes
What Class I, II, and III mean and which recalls demand immediate action.
What to Do When a Product Is Recalled
Verify, claim your remedy, report injuries, and navigate the process.
How to Check If Your Products Are Recalled
Step-by-step guide to checking food, products, medications, and vehicles.
Recalled Products in Your Home
A room-by-room household audit guide for active recalls.
Most Recalled Product Categories
Rankings of highest-recall categories from FDA, CPSC, and NHTSA.
Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
Explore related product safety and public health data from federal sources.
Food Safety Inspections
FDA and state food facility inspection results — violations, enforcement actions, and compliance history for food manufacturers and processors.
PlainFoodSafe →
Ingredient Safety Data
FDA food additive and ingredient safety database — regulatory status, usage limits, and safety assessments for thousands of ingredients.
PlainIngredients →
Nutrition Data
USDA nutrition facts for 2M+ food items — calories, macros, vitamins, and ingredient analysis to verify what you consume.
GetFoodFacts →
Drug Safety Information
FDA drug data for 680+ medications — interactions, alternatives, side effects, and safety information for recalled and active drugs.
PlainMeds →
Product Injury Data
CPSC emergency room injury data for 838 product categories — 7.3M NEISS records tracking real-world consumer product injuries.
PlainSafety →
Recall Checker
Search our database of 83K+ recalls by product name, brand, or recall number across all agencies.
Check Now →
Recall Radar
Live feed of the latest recalls across FDA, CPSC, NHTSA, and USDA — filter by agency and severity.
View Radar →
Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.
Zydus Pharmaceuticals (USA) Inc · 2026-03-18
· 2026-03-12
Cipla USA, Inc. · 2026-03-11
ACME UNITED CORPORATION · 2026-03-11
ACME UNITED CORPORATION · 2026-03-11
Compare this recall with Icosapent Ethyl Capsules, 1 gram, 120 Capsules per bottle, … →
Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).