# FDA recall D-0401-2026

> **Radnostix** · Class III · drug recall initiated 2026-02-19.

## Product

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 for recall

Failed Tablet/Capsule Specifications

## Distribution

Nationwide in the US, including Puerto Rico

## Key facts

- **Recall number:** D-0401-2026
- **Recalling firm:** Radnostix
- **Classification:** Class III
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2026-02-19
- **Report date:** 2026-04-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Idaho Falls, ID, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0401-2026

## Citation

> AI Analytics. FDA recall D-0401-2026. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0401-2026. Source: US FDA. Licensed CC0.

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