RecallRadar

FDA Drug recall D-0039-2027

Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial, 1 Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara - 39151…

On 2026-10-21 the FDA classified a Class II recall of Hydrocortisone Sodium Succinate for Injection, USP 100 mg/vial, 1 Vial, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Vadodara - 39151… by Zydus Pharmaceuticals Usa, citing failed Impurities/Degradation Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0039-2027
ClassificationClass II
Statusongoing
Initiated2026-10-01
Published2026-10-21
Last updated2026-10-27 05:30 UTC
CompanyZydus Pharmaceuticals Usa
DistributionUS

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.

Identifiers

ndc70710-1907-1
code_infoLot #: LB00047A, LB00048A, Exp. Date 03/2028

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-10-27 05:30 UTC. Current status: ongoing.

Other recalls by Zydus Pharmaceuticals Usa

All Zydus Pharmaceuticals Usa recalls

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0039-2027%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.