US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Apr 2, 2025 (17 months ago)

Haloperidol Decanoate Injection, 100 mg/mL*, 1 x 1 mL Single-Dose Vial, Rx only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of assurance of sterility. Bacterial contamination detected in some media fill units

What was recalled

Haloperidol Decanoate Injection, 100 mg/mL*, 1 x 1 mL Single-Dose Vial, Rx only, Manufactured by: Somerset Therapeutics Limited, #54/1, Boodhihal Village, Nelamangala, Bangalore - 562123, Karnataka, India, Manufactured for BluePoint Laboratories, NDC 68001-581-41.

Recalling firm
Amerisource Health Services LLC
NDC code
68001-581-41
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0368-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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