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TGA Action ID	RC-2025-RN-00366-1
Type of Product	Medicine
Product Name/Description	EverNatal 60 capsules Batch number: 43311 Exp: 01/27
ARTG Number	447572
Action Type	Recall
Action Level	Consumer
Hazard Classification	Class I
Reason for the Action	The ingredient potassium iodide included in the product was identified by the manufacturer as being more crystalline than usual which may result in a potential for a nonhomogeneous blend. This nonhomogeneous blend could lead to variability in dosing. The variability in dosing could lead to some units lacking the active ingredient while others may contain excessive amounts. Symptoms of iodine poisoning can range from mild to severe, depending on the level of iodine in the body. Mild symptoms consist of gastrointestinal upset, nausea, vomiting, and diarrhea, which may progress to more severe manifestations such as delirium, confusion, lethargy, and shock. There is also the potential for iodine deficiency if the product is lacking the active ingredient. This batch has been distributed to customers since 17th February 2025. No adverse events have been reported to date. This recall does not affect any other batches of EverNatal or any other Naternal Vitamin products.
Instructions for Customers/Users	Consumers: - Stop taking this product immediately - Return affected stock to the place of purchase for a refund or email Naternal Vitamins customer service on recall@naternalvitamins.com.au to arrange a replacement of affected product. Wholesalers/distributors: - Destroy stock and provide evidence of this in the response form for a refund or replacement. No alternative stock is available currently. Alternative stock is expected to be available in approximately 4 weeks from Naternal Vitamins. This action has been closed out on 09/07/2025
Action Commencement Date	1/04/2025
Responsible Entity	Naternal Vitamins
Contact Information	0420 972 736 - Naternal Vitamins