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Class II · ModerateActive recall

Hydrocortisone Sodium Succinate

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: LB00047A, LB00048A, Exp. Date 03/2028
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Failed Impurities/Degradation Specifications.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byZydus Lifesciences Ltd., Vadodara - 391510 India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534 foreign manufacturer
Brand nameHYDROCORTISONE SODIUM SUCCINATE
Generic nameHYDROCORTISONE SODIUM SUCCINATE
Active ingredient(s)HYDROCORTISONE SODIUM SUCCINATE
Distributed by / forZydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534
NDC70710-1907-1
Show the full FDA record
Full product labelHydrocortisone 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.
Recalling firmZydus Pharmaceuticals (USA) Inc
DistributionNationwide within the United States
Quantity70776 vials
Recall initiated2026-10-01
Report date2026-10-21
Recall completed—
Recall numberD-0039-2027
ClassificationClass II
FDA statusOngoing
Origin on filePennington NJ United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.