WhichRecall
Class IIIReported 2026-03-04

Eptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL Single-dose Vial, For Intravenous Use Only, Rx Only, Manufactured by: Hainan Poly Pharm. Co., Ltd., Guilinyang Economic Development Area, Haikou, Hainan Province, China 571127; Distributed by: Slate Run Pharmaceuticals, LLC, Columbus, Ohio 43215. NDC Slate Run Carton Label: 70436-027-80; NDC ProRx Carton Label: 70436-163-80

Recalled by Slate Run Pharmaceuticals

Reason for Recall

Labeling: Not Elsewhere Classified

Advertisement

The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.

Recall Number
D-0343-2026
Classification
Class III
Status
Ongoing
Category
drug
Initiated
2026-02-12
Reported
2026-03-04
Distribution
Nationwide within the USA.
Code Info
All lots within expiry
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
Advertisement