Radnostix recalls gelatin capsule packs for sodium iodide iodine-131 kits due to failed tablet specifications. Affected lots expire by February 2026 or September 2027. Consumers should check NDC numbers and lot dates.
Failed Tablet/Capsule Specifications
Radnostix is recalling gelatin capsule packs used with sodium iodide iodine-131 kits because the capsules may not meet required specifications. This could affect the safety and effectiveness of the medical treatment if used improperly.
The capsules may not meet required specifications, which could lead to improper medical treatment if used with the sodium iodide iodine-131 kit. This might affect the safety and effectiveness of the treatment.
Patients using the sodium iodide iodine-131 treatment kit with these specific gelatin capsule packs are affected. Those who have the recalled lots (NDC 69208-003-15, 69208-003-25, 69208-003-35) are most at risk.
Check for NDC numbers 69208-003-15, 69208-003-25, or 69208-003-35 on the packaging. The lot numbers are 3666245 (expiring 02/28/2026), 4546213 (expiring 02/28/2026), or 4951280 (expiring 09/30/2027).
Look for NDC numbers 69208-003-15, 69208-003-25, or 69208-003-35 and lot numbers 3666245, 4546213, or 4951280 on the packaging.
The capsules may not meet required specifications, which could affect the safety and effectiveness of the sodium iodide iodine-131 treatment.
NDC numbers 69208-003-15, 69208-003-25, and 69208-003-35 are affected.
Lot 3666245 expires February 28, 2026; Lot 4546213 expires February 28, 2026; Lot 4951280 expires September 30, 2027.
We’ve drafted a message you can send Radnostix to request your refund or repair — edit it as you like.
Subject: Recall D-0401-2026 — Radnostix Radnostix Hello, I own a Radnostix that is covered by recall D-0401-2026 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.
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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.
