QVAR (beclomethasone dipropionate HFA 40 mcg) recall: Impurity Out of Spec
QVAR (beclomethasone dipropionate HFA 40 mcg), 40 mcg Inhalation Aerosol, For Oral Inhalation with QVAR Actuator Only, 120 metered inhalations, Rx…
Why was QVAR (beclomethasone dipropionate HFA 40 mcg) recalled?
Failed Impurities/Degradation Specifications: out of specification test results for an impurity during stability testing.
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 #s:130449, 130450; Exp. Date: 12/2015
- Product
- QVAR (beclomethasone dipropionate HFA 40 mcg), 40 mcg Inhalation Aerosol, For Oral Inhalation with QVAR Actuator Only, 120 metered inhalations, Rx…
- Recalling firm
- Teva Pharmaceuticals USA
- Quantity
- 233,364 Inhalers
- Distribution
- Nationwide and Peurto Rico
- Recall date
- June 3, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)