QVAR¿ (beclomethasone dipropionate HFA) recall: Impurity Out of Spec
QVAR¿ (beclomethasone dipropionate HFA), C4 INHALATION AEROSOL in Aluminum Cylinders, Mktd by: Teva Respiratory, LLC, Horsham, PA 19044 Mfd by: 3M…
Why was QVAR¿ (beclomethasone dipropionate HFA) recalled?
Failed Impurity/Degradation Specification; for 17-BMP at the 9 and 18 month stability time point
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
lot 120088, exp.3/2014, NDC 59310-202-40, 40 mcg,8.7g / 120 metered inhalations, lot 120491, exp. 10/2014, NDC 59310-175-41,40 mcg,7.3g / 100 metered inhalations
- Product
- QVAR¿ (beclomethasone dipropionate HFA), C4 INHALATION AEROSOL in Aluminum Cylinders, Mktd by: Teva Respiratory, LLC, Horsham, PA 19044 Mfd by: 3M…
- Recalling firm
- Teva Pharmaceuticals USA
- Quantity
- 257,832 cylinders
- Distribution
- Nationwide
- Recall date
- April 9, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)