US Drug Recall Register
Class II · Moderate risk Terminated Initiated Sep 16, 2020 (6 years ago)

Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations…

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

Why it was recalled

Defective Delivery System: Sustained trend of failure to dispense complaints.

What was recalled

Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma Solutions, 160 N Pharma Drive, Morrisville, NC 27560, Distributed by: Perrigo, Allegan, MI 49010 NDC 45802-088-01

Recalling firm
Perrigo Company PLC
NDC code
45802-088-01
Origin
MI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1594-2020

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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