Foradil Aerolizer recall
Foradil Aerolizer (formoterol fumarate inhalation powder) 12 mcg per capsule, 12 Capsules (Blister strips of 6) per pack. For inhalation use only, Rx…
Why was Foradil Aerolizer recalled?
Failed Stability Specification: out of specification result obtained for the Particle Size Distribution test 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 #: F8011, Exp May 2015
- Product
- Foradil Aerolizer (formoterol fumarate inhalation powder) 12 mcg per capsule, 12 Capsules (Blister strips of 6) per pack. For inhalation use only, Rx…
- Recalling firm
- Novartis Pharmaceuticals Corp.
- Quantity
- 19,658 packs
- Distribution
- NJ via 1 distributor
- Recall date
- June 24, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)