Radnostix recalls Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit
- Recalling company
- Radnostix
- Product
- 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
- Reason
- Failed Tablet/Capsule Specifications
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- Feb 19, 2026
- Reported
- Apr 1, 2026
- Distribution
- Nationwide in the US, including Puerto Rico
- Status
- Ongoing
- Quantity
- 2,699 blister cartons
- Lot / codes
- Lot, expiry: Lot 3666245, exp: 02/28/2026; Lot 4546213, exp: 02/28/2026 and Lot 4951280, exp 09/30/2027
- Company location
- Idaho Falls, ID
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0401-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0401-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.