US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 24, 2015 (11 years ago)

COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray, 20 mcg/100 mcg…

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

Why it was recalled

Defective Delivery System: Inhalers do not spray properly, emitting either no spray or a short transient spray.

What was recalled

COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray, 20 mcg/100 mcg per actuation*, 4 Grams, 120 Metered Doses per inhaler, Rx only, Distributed by Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA, Made in Germany, NDC 0597-0024-02.

Recalling firm
Boehringer Ingelheim Roxane Inc
NDC code
0597-0024-02
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1279-2015

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.

Other Albuterol recalls

See all