PlainRecalls

NFH Iron Dietary Supplement Bottles Recalled Due to Risk of Poisoning; Violation of Federal Regulation for Child Resistant Packaging; Imported by Nutritional Fundamentals for Health (NFH)

Reported: March 27, 2025 Initiated: March 27, 2025 #25201 About 17,660 units

Nutritional Fundamentals for Health (dba NFH), of Canada issued this CPSC recall on March 27, 2025. Classified as Moderate severity. Approximately About 17,660 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 Pr…. 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.

Recall Insight

This CPSC action (record #25201) was formally reported on March 27, 2025. It is classified under Moderate severity, with a current status of Active. Nutritional Fundamentals for Health (dba NFH), of Canada is listed as the recalling firm. Federal records indicate About 17,660 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 is not child-resistant, posing a risk of poisoning if t… 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 secure the recalled supplement bottles out of sight and reach of children, and contact NFH for information on how to obtain a free replacement child-resistant bottle. NFH… — 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. 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 1 year 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.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

Units Affected

About 17,660

Related Recalls

6

0 from same agency

Product Description

This recall involves NFH Dietary Supplement bottles for Iron SAP, Heme Iron SAP and Prenatal SAP. The bottles are white with the brand name "NFH" and the firm's logo of a leaf in blue. The date code is on the bottom of the bottle. The recalled dietary supplement bottles have the following description and come in various sizes: Product Name Description Sizes Date Codes Iron SAP Iron Glycinate 60 Capsules (1029U) 120 Capsules (1167U) 60 capsules 5398705/31/2027 5398805/31/2027 5398512/31/2026 5398612/31/2026 5398306/30/2026 5398406/30/2026 N00274 07/31/2025 120 capsules 538975/31/2027 539875/31/2027 539885/31/2027 5398512/31/2026 5398612/31/2026 539846/30/2026 N00274 6/30/2025 Heme Iron SAP (Porcine) Superior Absorption and Bioavailability 60 Capsules (1124U) N00265 - 03/31/2025 53809 - 05/31/2026 53810 - 07/31/2026 57807 - 10/30/2026 53811 - 10/31/2026 57806 - 10/31/2026 62379 - 08/31/2027 Prenatal SAP Multivitamin 180 Capsules (1034U) 5821709/30/2027 5822009/30/2027 5736105/31/2027 5736905/31/2027 5737005/31/2027 5737205/31/2027 5821405/31/2027 5396803/31/2027 5719401/31/2027 5736001/31/2027 5396311/30/2026 5396411/30/2026 5396511/30/2026 5396611/30/2026 5396711/30/2026 5395410/31/2026 5395610/31/2026 5395810/31/2026 5396010/31/2026 5396110/31/2026 5396210/31/2026 5395307/31/2026 5394605/31/2026 5394504/30/2026 N00287 08/31/2025 N00285 04/30/2025 N00284 03/31/2025

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 is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.

Remedy

Consumers should immediately secure the recalled supplement bottles out of sight and reach of children, and contact NFH for information on how to obtain a free replacement child-resistant bottle. NFH is contacting all known purchasers directly. This recall only includes the bottle.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 25201
Date reported March 27, 2025
Date initiated March 27, 2025
Recalling firm Nutritional Fundamentals for Health (dba NFH), of Canada
Units affected About 17,660
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

About 17,660 units affected — limited or regional distribution scale.

Regional (<10K units)
Multi-state (10K – 100K units) ✓ This recall
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. Consumer Product Safety Commission filings.

Frequently Asked Questions

What product was recalled?
This recall involves NFH Dietary Supplement bottles for Iron SAP, Heme Iron SAP and Prenatal SAP. The bottles are white with the brand name "NFH" and the firm's logo of a leaf in blue. The date code is on the bottom of the bottle. The recalled dietary supplement bottles have the following description and come in various sizes: Product Name Description Sizes Date Codes Iron SAP Iron Glycinate 60 Capsules (1029U) 120 Capsules (1167U) 60 capsules 5398705/31/2027 5398805/31/2027 5398512/31/2026 5398612/31/2026 5398306/30/2026 5398406/30/2026 N00274 07/31/2025 120 capsules 538975/31/2027 539875/31/2027 539885/31/2027 5398512/31/2026 5398612/31/2026 539846/30/2026 N00274 6/30/2025 Heme Iron SAP (Porcine) Superior Absorption and Bioavailability 60 Capsules (1124U) N00265 - 03/31/2025 53809 - 05/31/2026 53810 - 07/31/2026 57807 - 10/30/2026 53811 - 10/31/2026 57806 - 10/31/2026 62379 - 08/31/2027 Prenatal SAP Multivitamin 180 Capsules (1034U) 5821709/30/2027 5822009/30/2027 5736105/31/2027 5736905/31/2027 5737005/31/2027 5737205/31/2027 5821405/31/2027 5396803/31/2027 5719401/31/2027 5736001/31/2027 5396311/30/2026 5396411/30/2026 5396511/30/2026 5396611/30/2026 5396711/30/2026 5395410/31/2026 5395610/31/2026 5395810/31/2026 5396010/31/2026 5396110/31/2026 5396210/31/2026 5395307/31/2026 5394605/31/2026 5394504/30/2026 N00287 08/31/2025 N00285 04/30/2025 N00284 03/31/2025. Recalled by Nutritional Fundamentals for Health (dba NFH), of Canada. Units affected: About 17,660.
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 is not child-resistant, posing a risk of poisoning if the contents are swallowed by young children.
What should consumers do?
Consumers should immediately secure the recalled supplement bottles out of sight and reach of children, and contact NFH for information on how to obtain a free replacement child-resistant bottle. NFH is contacting all known purchasers directly. This recall only includes the bottle.
Which agency issued this recall?
This recall was issued by the CPSC on March 27, 2025. Severity: Moderate. Recall number: 25201.
How do I check if my product is affected by a recall?
Check the product description and recall number (25201) 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.

Recall Context

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.

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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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

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.

All federal data sources used on this page

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).