US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Mar 21, 2025 (1 years ago)

Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by…

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

Why it was recalled

Lack of Assurance of Sterility: Media fill with bacterial contamination

What was recalled

Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited, Kamataka India, Manufactured for: BluePoint Laboratories NDC 68001-580-41

Recalling firm
Somerset Therapeutics Private Limited
NDC code
68001-580-41
Origin
N/A, India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0356-2025

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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