California Gold Nutrition Iron Supplements: Daily Prenatal Multi, Ultamins Women's Multivitamin, and Ultamins Women's 50
Summary
CPSC recall: California Gold Nutrition Iron Supplements: Daily Prenatal Multi, Ultamins Women's Multivitamin, and Ultamins Women's 50+ Multivitamin. By iHerb LLC, dba Madre Labs LLC, of Irvine, California. Hazard: 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 pack
Details
Source
CPSC Consumer Product Recall
External ID
10320
Action Date
2025-06-26
Status
Recalled
Category
consumer_product
Product Description
This recall involves three types of California Gold Nutrition dietary supplements: Daily Prenatal Multi, Ultamins Women'
Context & Analysis
This is a unclassified recall.
This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
iHerb LLC, dba Madre Labs LLC, of Irvine, California has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (iHerb LLC, dba Madre Labs LLC, of Irvine, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does iHerb LLC, dba Madre Labs LLC, of Irvine, California have FDA actions?
iHerb LLC, dba Madre Labs LLC, of Irvine, California has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10320" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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