Radnostix: Sodium Iodide (I-131) Solution, Therapeutic Oral, packaged as a) 1 ml V-vial, NDC 69208-003-15; Order 49317, 49323, 49325, 49329, 49333, 493
Read the official notice at FDA (drug) →
The text below is copied from the official FDA (drug) record. If anything differs, the official notice is correct.
- Company / brand
- Radnostix
- 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 / hazard
- Presence of Particulate Matter: Due to production issues
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- Nationwide in the USA and Puerto Rico
- Recall initiated
- 2026-01-26
- Code info
- Batch I012626R-01, Exp 02/09/2026
- Product quantity
- 16 units
- Voluntary mandated
- Voluntary: Firm initiated
- City
- Idaho Falls
- State
- ID
- Country
- United States
- Event id
- 98470
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