WhichRecall
Class IIReported 2026-03-11

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.

Recalled by Radnostix

Reason for Recall

Presence of Particulate Matter: Due to production issues

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Recall Number
D-0389-2026
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2026-01-26
Reported
2026-03-11
Distribution
Nationwide in the USA and Puerto Rico
Code Info
Batch I012626R-01, Exp 02/09/2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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