Radnostix recalls

Radnostix has 2 recalls on record with the FDA and USDA, the earliest in 2026 and the latest reported on 1 Apr 2026. 2 are still ongoing. 2 were reported in the last 12 months. The most frequent reason is particulate matter.

Total recalls2since 2026

Last 12 months2reported

Class I00% of total

Ongoing2latest 1 Apr 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 1 1 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 1 50%Class III 1 50%

Why radnostix is recalled

Particulate Matter150%
Packaging Defects150%

Product types

Injectable & IV Drugs150%

By year

20262100%

Ongoing radnostix recalls

2 active

Reported	Class	Recall	Company	Reason	Where
1 Apr 2026Drug	CLASS III	Gelatin Capsule Pack for use recalled by RadnostixSodium Iodide I-131	Radnostix	Packaging Defects	Nationwide
11 Mar 2026Drug	CLASS II	Sodium Iodide (I-131) Solution, Therapeutic Oral recalled by RadnostixSodium Iodide I-131	Radnostix	Particulate Matter	Nationwide

All radnostix recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
1 Apr 2026Drug	CLASS III	Gelatin Capsule Pack for use recalled by RadnostixSodium Iodide I-131	Radnostix	Packaging Defects	Nationwide
11 Mar 2026Drug	CLASS II	Sodium Iodide (I-131) Solution, Therapeutic Oral recalled by RadnostixSodium Iodide I-131	Radnostix	Particulate Matter	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.