FDA Drug Recalls

Recalls / Class III

Class IIID-0171-2017

Product

Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg, 50 Metered Sprays, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044, By: 3M Drug Delivery Systems, Northridge, CA 91324, NDC 59310-210-13.

Affected lot / code info
Lot #: 150335, 150336, Exp. 4/2017

Why it was recalled

Failed Content Uniformity: Product was out of specification for spray content uniformity obtained during stability testing.

Recalling firm

Firm
Teva Pharmaceuticals USA
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1090 Horsham Rd, N/A, North Wales, Pennsylvania 19454-1505

Distribution

Quantity
N/A
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-11-01
FDA classified
2016-12-08
Posted by FDA
2016-12-14
Terminated
2018-02-06
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0171-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.