Zydus Pharmaceuticals (USA) Inc: Drug Recall

Recall #D-0153-2026 · 10/22/2025

Class II: Risk

Recall Details

Recall Number
D-0153-2026
Classification
Class II
Product Type
Drug
Recalling Firm
Zydus Pharmaceuticals (USA) Inc
Status
Ongoing
Date Initiated
10/22/2025
Location
Pennington, NJ, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Reason for Recall

cGMP deviations: an observed Out of Specification of Nitrosamine Drug Substance-Related Impurities (NDSRIs), N-Nitroso Desmethyl-Clomipramine, above the FDA acceptable intake limit.

Product Description

clomiPRAMINE Hydrochloride, Capsules, USP, 50 mg, packaged in a) 30-count bottles (NDC 16714-850-01), b) 90-count bottles (NDC 16714-850-02), c) 100-count bottles (NDC 16714-850-03), Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India

Distribution Pattern

Nationwide in the US

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.