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CPSC recall · Reported June 26, 2025

iHerb Recalls Bottles and Blister Packs of California Gold Nutrition Iron Supplements Due to Risk of Serious Injury or Death from Child Poisoning; Violation of Federal Standard for Child Resistant Packaging

The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The iron-containing dietary suppleme…

Recall #
25354
Affected scope
About 60,000
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iHerb LLC, dba Madre Labs LLC, of Irvine, California recalled This recall involves three types of California Gold Nutrition dietary supplements: Daily ….

iHerb Recalls Bottles and Blister Packs of California Gold Nutrition Iron Supplements Due… was recalled by iHerb LLC, dba Madre Labs LLC, of Irvine, California in June 26, 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 #25354 with the CPSC before acting.

The recall

iHerb LLC, dba Madre Labs LLC, of Irvine, California issued this CPSC recall-The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the….

None
agency class
June 26, 2025
reported

Sourced from official CPSC enforcement records. Verify recall #25354 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. Consumers holding this product should act on the agency's documented remedy above 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.

Food recalls over time

Where this recall sits in its category - 25,457 food recalls on record

01,0002,0003,000 20052008201120142017202020232026 813

Product description

This recall involves three types of California Gold Nutrition dietary supplements: Daily Prenatal Multi, Ultamins Women's Multivitamin, and Ultamins Women's 50+ Multivitamin. The California Gold Nutrition Daily Prenatal Multivitamin bottles are white with a white lid and a gold border label. The bottle contains 60 fish gelatin softgel dietary supplements. The California Gold Nutrition Women's Multivitamin and Women's 50+ Multivitamin both have dark purple packaging with a gold border label. Both products contain 60 capsules in foil within the packaging. The following batch numbers and expiration dates for the products are printed on the back of the package near the bottom of package/sleeve. Products Batch Codes Expiration Dates Daily Prenatal Multi 2307050A, 2404096A, 2411100A 08/2025, 05/2026, 11/2026 Ultamins Women's Multivitamin V0532, V0533 11/2026, 07/2026 Ultamins Women's 50+ Multivitamin V0534, V0536 07/2026, 11/2026

Reason for recall

The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The iron-containing dietary supplement packages violate the federal standard for child-resistant packaging because the bottles and blister packs are not child-resistant, posing a risk of deadly 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 iHerb for a refund and information on how to safely discard the packaging and product. To receive a refund, consumers should email ProductRecall@iherb.com with the subject line: "Iron Supplement Refund" and provide the following information: Name; Product(s) name & quantity ordered; Evidence of destruction: initial and date each product package and include a photo with your initials and the date visible; Optional: Provide the order number associated with the purchase(s), which can be found by logging into consumer's account and viewing the "Order History". iHerb is contacting all known purchasers directly.

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Not classified by agency
Status Active
Recall number 25354
Date reported June 26, 2025
Date initiated June 26, 2025
Recalling firm iHerb LLC, dba Madre Labs LLC, of Irvine, California
Affected scope About 60,000
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 secure the recalled supplement bottles out of sight and reach of children and contact iHerb for a re…

  • Check the recall number (25354) 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 three types of California Gold Nutrition dietary supplements: Daily Prenatal Multi, Ultamins Women's Multivitamin, and Ultamins Women's 50+ Multivitamin. The California Gold Nutrition Daily Prenatal Multivitamin bottles are white with a white lid and a gold border label. The bottle contains 60 fish gelatin softgel dietary supplements. The California Gold Nutrition Women's Multivitamin and Women's 50+ Multivitamin both have dark purple packaging with a gold border label. Both products contain 60 capsules in foil within the packaging. The following batch numbers and expiration dates for the products are printed on the back of the package near the bottom of package/sleeve. Products Batch Codes Expiration Dates Daily Prenatal Multi 2307050A, 2404096A, 2411100A 08/2025, 05/2026, 11/2026 Ultamins Women's Multivitamin V0532, V0533 11/2026, 07/2026 Ultamins Women's 50+ Multivitamin V0534, V0536 07/2026, 11/2026. Recalled by iHerb LLC, dba Madre Labs LLC, of Irvine, California. Units affected: About 60,000.
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. The iron-containing dietary supplement packages violate the federal standard for child-resistant packaging because the bottles and blister packs are not child-resistant, posing a risk of deadly 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 iHerb for a refund and information on how to safely discard the packaging and product. To receive a refund, consumers should email ProductRecall@iherb.com with the subject line: "Iron Supplement Refund" and provide the following information: Name; Product(s) name & quantity ordered; Evidence of destruction: initial and date each product package and include a photo with your initials and the date visible; Optional: Provide the order number associated with the purchase(s), which can be found by logging into consumer's account and viewing the "Order History". iHerb is contacting all known purchasers directly.
Which agency issued this recall?
This recall was issued by the CPSC on June 26, 2025. CPSC does not publish a hazard classification for this recall. Recall number: 25354.
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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This recall: CPSC, reported June 26, 2025. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026