PlainRecalls
FDA Drug Moderate Class II Terminated

QVAR¿ (beclomethasone dipropionate HFA), 80mcg Inhalation Aerosol, 50 metered inhalations/120 metered inhalations, packaged in an aluminum cylinder, Mktd. by: Teva Respiratory, LLC, Horsham, PA, Mfd. by: 3M Drug Delivery Systems, Northridge, CA.

Reported: May 28, 2014 Initiated: April 23, 2014 #D-1341-2014

Product Description

QVAR¿ (beclomethasone dipropionate HFA), 80mcg Inhalation Aerosol, 50 metered inhalations/120 metered inhalations, packaged in an aluminum cylinder, Mktd. by: Teva Respiratory, LLC, Horsham, PA, Mfd. by: 3M Drug Delivery Systems, Northridge, CA.

Reason for Recall

Defective Delivery System; defective valve

Details

Recalling Firm
Teva Pharmaceuticals USA
Units Affected
461,592 canisters
Distribution
Nationwide
Location
Horsham, PA

Frequently Asked Questions

What product was recalled?
QVAR¿ (beclomethasone dipropionate HFA), 80mcg Inhalation Aerosol, 50 metered inhalations/120 metered inhalations, packaged in an aluminum cylinder, Mktd. by: Teva Respiratory, LLC, Horsham, PA, Mfd. by: 3M Drug Delivery Systems, Northridge, CA.. Recalled by Teva Pharmaceuticals USA. Units affected: 461,592 canisters.
Why was this product recalled?
Defective Delivery System; defective valve
Which agency issued this recall?
This recall was issued by the FDA Drug on May 28, 2014. Severity: Moderate. Recall number: D-1341-2014.