Recall RadarSodium 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. (…
Presence of Particulate Matter: Due to production issues
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- Radnostix — Idaho Falls, ID
- Severity
- Class II — moderate
- Reported
- March 11, 2026
- Quantity
- 16 units
- Recall number
- D-0389-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Nationwide in the USA and Puerto Rico
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