Shenzhen Techdow Pharmaceutical Co., Ltd. recalls Heparin Sodium Injection
- Recalling company
- Shenzhen Techdow Pharmaceutical Co., Ltd.
- Product
- 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
- Lack of Assurance of Sterility
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 1, 2026
- Reported
- Oct 28, 2026
- Distribution
- Nationwide in the USA.
- Status
- Ongoing
- Quantity
- 251,000 1 mL multidose vials
- Lot / codes
- Lot# CU03232A, Exp 1/31/2028
- Company location
- Shenzhen
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0050-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0050-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.