Recall
FDAHealthJanuary 26, 2026

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, 49339, 49341,49355, 49364, 49380, 49392. (b) 2 ml

⚠️ Presence of Particulate Matter: Due to production issues

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
January 26, 2026

Nationwide in the USA and Puerto Rico

What's affected?

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.
Lot code
Batch I012626R-01, Exp 02/09/2026

Additional details

Batch I012626R-01, Exp 02/09/2026

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 16 units.

View original FDA notice →

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