Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (cont…
Recalled by Radnostix
Class III — least serious
Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
Radnostix has recalled Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (cont…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 1, 2026 and was initiated on February 19, 2026. It is classified as a Class III recall, which means using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (cont…, with approximately 2,699 blister cartons affected. The company behind the recall is Radnostix, based in Idaho Falls, ID. The FDA describes the product as: “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 was Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (cont… recalled?
According to the FDA, the stated reason for the recall is: “Failed Tablet/Capsule Specifications.”
What should you do?
If you think you may have bought Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (cont…, compare it against the product description and identifying codes (Lot, expiry: Lot 3666245, exp: 02/28/2026; Lot 4546213, exp: 02/28/2026 and Lot 4951280, exp 09/30/2027) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Radnostix or your local health authority.
About this recall
This recall was distributed in ID. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- April 1, 2026
- Recall started
- February 19, 2026
- Distributed in
- ID
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (cont… recalled?+
According to the FDA: Failed Tablet/Capsule Specifications
How serious is this recall?+
Class III — least serious. Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
What should I do if I have Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit (cont…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: D-0401-2026. Information last synced from the FDA on July 5, 2026.