HIGHFDA DRUG
Radnostix Sodium Iodide I-131 Gel Capsule Pack Recalled for 2,699 Units in 2026
Radnostix recalled 2,699 gelatin capsule packs used with its Sodium Iodide I-131 kit, distributed nationwide in the United States and Puerto Rico. The capsules failed to meet tablet/capsule specifications. Healthcare providers and patients should stop using the product and contact Radnostix for guidance.
SODIUM IODIDE I-131
Failed Tablet/Capsule