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Recalls → D-0050-2027
Class II Recall · D-0050-2027 Report Date: 2026-10-28 · Status: Ongoing

Shenzhen Techdow Pharmaceutical Co., Ltd. — EPA / Specialty Chemical Recall

Product Description: Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1mL Multi dose vial x 25 vials per carton, Distributed by: Hepalink USA Inc., Langhome, PA 19047-1885. Carton NDC: NDC 81952-111-06, Vial NDC: 81942-111-01
Reason for Recall: Lack of Assurance of Sterility
Distribution Pattern: Nationwide in the USA.
View Linked Facility Profile (FEI FEI-5B4DCDE8) → Verify on openFDA ↗