US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 30, 2025 (14 months ago)

Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per…

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

Why it was recalled

Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.

What was recalled

Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for: Ciple USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC# 69097-319-86 (pouch), 69097-319-87 (carton)

Recalling firm
Cipla USA, Inc.
NDC code
69097-319-86
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0541-2025

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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