Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Heparin Sodium Injection Recalled by Sagent Pharmaceuticals Inc Due to Labeling: Not elsewhere classified
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 Sagent Pharmaceuticals Inc directly.
Affected Products
Heparin Sodium Injection, USP, 20,000 USP units per mL, 25 x 1 mL Multi-Dose Vials, Rx Only, For Intravenous or Subcutaneous Use, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195; Made in India, NDC carton: 25021-404-01
Quantity: 28,875 vials
Why Was This Recalled?
Labeling: Not elsewhere classified
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sagent Pharmaceuticals Inc
Sagent Pharmaceuticals Inc has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report