Severity
Moderate
CPSC recall · Reported June 26, 2025
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…
iHerb LLC, dba Madre Labs LLC, of Irvine, California recalled This recall involves three types of California Gold Nutrition dietary supplements: Daily … - a moderate-severity action.
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 moderate-severity CPSC recall-The recalled dietary supplements contain iron, which must be in child-resistant packaging, as required by the….
Sourced from official CPSC enforcement records. Verify recall #25354 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This CPSC action (record #25354) was formally reported on June 26, 2025. It is classified under Moderate severity, with a current status of Active. iHerb LLC, dba Madre Labs LLC, of Irvine, California is listed as the recalling firm. Federal records list the affected scope as About 60,000.
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. The iron-containing dietary supplement packages violate the federal standard… 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 iHerb for a refund and information on how to safely discard the packaging and produc… - 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, 4 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 its category - 25,126 food 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.
Severity
Moderate
Affected scope
About 60,000
Related Recalls
6
4 from same agency
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
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.
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.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| 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…
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.
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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 26, 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.