Eptifibatide recalls

The FDA has published 6 recalls involving Eptifibatide since 2016. The latest was reported on 4 Mar 2026. Most were for potency & assay. Akorn has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls6since 2016

Last 12 months1reported

Class I00% of total

Ongoing2latest 4 Mar 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 1 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 1 17%Class III 5 83%

Why eptifibatide is recalled

Companies

By year

2026117%
2024117%
2019350%
2016117%

Ongoing eptifibatide recalls

2 active

Reported	Class	Recall	Company	Reason	Where
4 Mar 2026Drug	CLASS III	Eptifibatide Injection, 75 mg/ vial recalledEptifibatide	Slate Run Pharmaceuticals	Other	Nationwide
26 Jun 2024Drug	CLASS III	Eptifibatide injection 20mg/ (2mg/mL) Single-Dose Vial recalledEptifibatide	Eugia US	Potency & Assay	Nationwide

All eptifibatide recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
4 Mar 2026Drug	CLASS III	Eptifibatide Injection, 75 mg/ vial recalledEptifibatide	Slate Run Pharmaceuticals	Other	Nationwide
26 Jun 2024Drug	CLASS III	Eptifibatide injection 20mg/ (2mg/mL) Single-Dose Vial recalledEptifibatide	Eugia US	Potency & Assay	Nationwide
4 Sep 2019Drug	CLASS III	Eptifibatide Injection, 75 mg/ 75 mg/mL) Single-use Vial recalled	Akorn	Potency & Assay	Nationwide
4 Sep 2019Drug	CLASS III	Eptifibatide Injection, a) 20 mg/ (2 mg/mL) Single Use Vial recalled	Akorn	Potency & Assay	Nationwide
4 Sep 2019Drug	CLASS III	Eptifibatide Injection, 75 mg/ 75 mg/mL) Single-use Vial recalled	Akorn	Potency & Assay	Nationwide
14 Sep 2016Drug	CLASS II	Eptifibatide Injection 75 mg/ 75 mg/mL) single use vial recalled	Teva North America	Manufacturing (CGMP) Deviations	Nationwide

Should you stop taking Eptifibatide?

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.