Drug recall D-0389-2026
Product
Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC 69208-003-15; Order 49317, 49323, 49325, 49329, 49333, 49339, 49341,49355, 49364, 49380, 49392. (b) 2 ml V-Vial, NDC 69208-003-25; Order 49353,49457, 49477. (c) 3 ml V-vial, NDC 69208-003-35; Order 49454,49406. Rx Only, Manufactured by: International Isotopes Inc., Idaho Falls, ID.
Reason for recall
Presence of Particulate Matter: Due to production issues
Lots and codes
Batch I012626R-01, Exp 02/09/2026
Recall details
- Recalling firm
- Radnostix, Idaho Falls, ID
- Quantity
- 16 units
- Distribution
- Nationwide in the USA and Puerto Rico
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 26, 2026
Related products
- Sodium Iodide I-131 – drug information
- NDC 69208-000 Sodium Iodide I-131 · · Radnostix, Inc.