Perampanel recalls

The FDA has published 1 recall involving Perampanel since 2026. The latest was reported on 1 Jul 2026. Most were for packaging defects. 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 1 Jul 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 0 0 0May 0 1 0Aug 0 0

Severity split

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

Why perampanel is recalled

Packaging Defects1100%

Companies

SUN Pharmaceutical Industries1100%

By year

20261100%

Ongoing perampanel recalls

1 active

Reported	Class	Recall	Company	Reason	Where
1 Jul 2026Drug	CLASS II	Perampanel CIII Tablets, 6mg recalled by Sun Pharmaceutical IndustriesPerampanel	SUN Pharmaceutical Industries	Packaging Defects	Nationwide

All perampanel recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
1 Jul 2026Drug	CLASS II	Perampanel CIII Tablets, 6mg recalled by Sun Pharmaceutical IndustriesPerampanel	SUN Pharmaceutical Industries	Packaging Defects	Nationwide

Should you stop taking Perampanel?

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.