Exenatide recalls

The FDA has published 1 recall involving Exenatide since 2026. The latest was reported on 30 Sep 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 30 Sep 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 0 0Aug 1 0

Severity split

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

Why exenatide is recalled

Other Reasons1100%

Companies

Amneal Pharmaceuticals of New York1100%

By year

20261100%

Ongoing exenatide recalls

1 active

Reported	Class	Recall	Company	Reason	Where
30 Sep 2026Drug	CLASS II	Exenatide Injection, USP, 250 mcg/mL per prefilled pen recalledExenatide	Amneal Pharmaceuticals of New York	Other	Nationwide

All exenatide recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
30 Sep 2026Drug	CLASS II	Exenatide Injection, USP, 250 mcg/mL per prefilled pen recalledExenatide	Amneal Pharmaceuticals of New York	Other	Nationwide

Should you stop taking Exenatide?

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.