Radnostix recalls Sodium Iodide (I-131) Solution due to particulate matter from production issues. This therapeutic oral solution is for medical use only and requires immediate attention.
Presence of Particulate Matter: Due to production issues
Radnostix has recalled specific batches of Sodium Iodide (I-131) Solution, a therapeutic oral medication, because production issues caused particulate matter. This could pose a risk to patients using the product.
Particulate matter in the solution could cause harm if injected or ingested, as it may lead to blockages or other complications in the body. The production issues resulted in small particles being present in the medication.
Patients prescribed Sodium Iodide (I-131) Solution by a healthcare provider are affected. Those using the recalled batches for medical treatment are at risk.
Check for the product name 'Sodium Iodide (I-131) Solution, Therapeutic Oral' with the specific NDC codes and order numbers listed in the recall notice. The product is only available by prescription.
Verify the NDC code and order numbers listed in the recall notice to confirm if your product is affected.
The recall states that the product contains particulate matter due to production issues, so it is not safe to use as intended.
The recall does not specify a remedy, so contact your healthcare provider for guidance on next steps.
Check the NDC code (69208-003-15 for 1 ml vial) and order numbers listed in the recall notice.
We’ve drafted a message you can send Radnostix to request your refund or repair — edit it as you like.
Subject: Recall D-0389-2026 — Radnostix Radnostix Hello, I own a Radnostix that is covered by recall D-0389-2026 from Radnostix. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
