Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit recall (Radnostix)
DrugClass IIIOngoing
Summary: Radnostix is recalling Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35. Reason: Failed Tablet/Capsule Specifications.
What is being recalled
Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (containing 5 empty capsules and 5 Dibasic Sodium Phosphate Capsules 300 mg, International Isotopes Inc., Idaho Falls, ID 83401. NDC: 69208-003-15; 69208-003-25; 69208-003-35
Why
Failed Tablet/Capsule Specifications
How serious is it
Class III is the least serious level: using or being exposed to this product is not likely to cause health problems, but it breaks FDA rules.
Where it was sold
Nationwide in the US, including Puerto Rico (states named: Puerto Rico)
How to tell if yours is affected
Lot, expiry: Lot 3666245, exp: 02/28/2026; Lot 4546213, exp: 02/28/2026 and Lot 4951280, exp 09/30/2027
What to do
Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.
Recall facts
| Recall number | D-0401-2026 |
| Category | Drug |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class III |
| Status | Ongoing |
| Recall started | February 19, 2026 |
| Reported | April 1, 2026 |
| Company | Radnostix |
| Company location | Idaho Falls, ID, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 2,699 blister cartons |
More recalls from Radnostix · all drug recalls · recalls from February 2026