Haloperidol Decanoate Injection recalled over sterility concerns
- Recall date
- March 21, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Somerset Therapeutics Private Limited recalls Haloperidol Decanoate Injection, 100 mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured for: Somerset Therapeutics, LLC…
- Recall number
- D-0358-2025
- FDA classification
- Class II
- Brand / firm
- Somerset Therapeutics Private Limited
- Sold / distributed
- U.S. Nationwide
Why it was recalled
Lack of Assurance of Sterility: Media fill with bacterial contamination
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Haloperidol Decanoate Injection, 100 mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Somerset, NJ 08873, NDC 70069-383-10
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