Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Eptifibatide Injection Recalled by Slate Run Pharmaceuticals Due to Labeling: Not Elsewhere Classified. The carton for Eptifibatide...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Slate Run Pharmaceuticals directly.
Affected Products
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
Quantity: N/A
Why Was This Recalled?
Labeling: Not Elsewhere Classified. 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Slate Run Pharmaceuticals
Slate Run Pharmaceuticals has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report