FDAFDA · Food and drugs·Recall number D-0401-2026
Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35
Published April 1, 2026 · Recall initiated: February 19, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM IODIDE I-131
- Manufacturer
- Radnostix
- Distributor
- Nationwide in the US, including Puerto Rico
- Lot
- Lot, expiry: Lot 3666245, exp: 02/28/2026; Lot 4546213, exp: 02/28/2026 and Lot 4951280, exp 09/30/2027
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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