Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
QVAR¿ (beclomethasone dipropionate HFA) Recalled by Teva Pharmaceuticals USA Due to Failed Impurity/Degradation Specification; for 17-BMP at the 9...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA directly.
Affected Products
QVAR¿ (beclomethasone dipropionate HFA), C4 INHALATION AEROSOL in Aluminum Cylinders, Mktd by: Teva Respiratory, LLC, Horsham, PA 19044 Mfd by: 3M Drug Delivery Systems, Northridge, CA 91324.
Quantity: 257,832 cylinders
Why Was This Recalled?
Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month stability time point
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report