US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 3, 2018 (8 years ago)

Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30

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

Why it was recalled

Lack of Processing Controls.

What was recalled

Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30

Recalling firm
Kroger Specialty Pharmacy, Inc.
NDC code
76204-0200-60
Origin
MS, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0735-2018

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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