ModerateActive

CPSC recall · Reported March 27, 2025

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)

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-re…

Recall #: 25201
Affected scope: About 17,660

Compiled from official public sources by the editorial team. · Updated July 2026

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Nutritional Fundamentals for Health (dba Nfh), of Canada recalled This recall involves NFH Dietary Supplement bottles for Iron SAP, Heme Iron SAP and Prena… - a moderate-severity action.

NFH Iron Dietary Supplement Bottles Recalled Due to Risk of Poisoning; Violation of Feder… was recalled by Nutritional Fundamentals for Health (dba Nfh), of Canada in March 27, 2025. Reason: The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the…. Remedy: Consumers should immediately secure the recalled supplement bottles out of sight and reac…. Verify recall #25201 with the CPSC before acting.

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The recall

Nutritional Fundamentals for Health (dba Nfh), of Canada issued this moderate-severity CPSC recall-The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the….

Moderate
severity level: March 27, 2025
reported

Sourced from official CPSC enforcement records. Verify recall #25201 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

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 list the affected scope as About 17,660.

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.

Within the same product category the archive holds 6 closely related recalls, 6 from CPSC - 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.

Where this recall sits in the database

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.

Severity

Moderate

Affected scope

About 17,660

Related Recalls

6 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, what to 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.

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
Affected scope	About 17,660
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 secure the recalled supplement bottles out of sight and reach of children, and contact NFH for infor…

Check the recall number (25201) 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? ▼

Why was this product recalled? ▼

What should consumers do? ▼

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.

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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 March 27, 2025. 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.