Abiraterone recalls

The FDA has published 1 recall involving Abiraterone since 2026. The latest was reported on 28 Oct 2026. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2026

Last 12 months1reported

Class I00% of total

Ongoing1latest 28 Oct 2026

Recalls per month, last 24 months

click a bar for that month

0Dec '24 0 0 0Mar 0 0 0Jun 0 0 0Sep 0 0 0Dec 0 0 0Mar 0 0 0Jun 0 0 0Sep 1 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why abiraterone is recalled

Other Reasons1100%

Companies

Hikma Pharmaceuticals USA1100%

By year

20261100%

Ongoing abiraterone recalls

1 active

Reported	Class	Recall	Company	Reason	Where
28 Oct 2026Drug	CLASS II	Abirtega (abiraterone acetate) USP, 250 mg recalledAbirtega	Hikma Pharmaceuticals USA	Other	Nationwide

All abiraterone recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
28 Oct 2026Drug	CLASS II	Abirtega (abiraterone acetate) USP, 250 mg recalledAbirtega	Hikma Pharmaceuticals USA	Other	Nationwide

Should you stop taking Abiraterone?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.