Class II · Moderate riskTerminated Initiated Dec 26, 2014 (12 years ago)
Dehydrated alcohol vials
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of sterility assurance.
What was recalled
Dehydrated alcohol vials
Recalling firm
Walgreens Infusion Services
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0371-2015
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.