FDA recall record

Teva Pharmaceuticals USA Qnasl recall — FDA D-0171-2017

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

Class IIIclassification
D-0171-2017official record ID
Dec 14, 2016report date

Recall record at a glance

Official recordD-0171-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTeva Pharmaceuticals USA
Report dateDec 14, 2016
Recall initiation dateNov 1, 2016
QuantityN/A
LocationNorth Wales, PA, United States

Official product description

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.

Why the product was recalled

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

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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