US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 28, 2016 (10 years ago)

Sclerosol Intrapleural Aerosol (sterile talc powder), Intrapleural administration, 4 g…

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

Why it was recalled

Defective Delivery System: Defective stem valve causes leakage of the propellant in the spray canister delivering no drug or an inadequate amount of the drug to be delivered.

What was recalled

Sclerosol Intrapleural Aerosol (sterile talc powder), Intrapleural administration, 4 g Canister, Rx Only, Distributed by: Bryan Corporation, Woburn, MA 01801, USA, NDC 63256-100-30

Recalling firm
Lymol Medical
NDC code
63256-100-30
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0858-2016

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.