Zydus Pharmaceuticals (USA) Inc recalls Hydrocortisone Sodium Succinate for Injection
- Recalling company
- Zydus Pharmaceuticals (USA) Inc
- Product
- Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial, 1 Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara - 391510 India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1907-1.
- Reason
- Failed Impurities/Degradation Specifications.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 1, 2026
- Reported
- Oct 21, 2026
- Distribution
- Nationwide within the United States
- Status
- Ongoing
- Quantity
- 70776 vials
- Lot / codes
- Lot #: LB00047A, LB00048A, Exp. Date 03/2028
- Company location
- Pennington, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0039-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0039-2027 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.