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.
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