PlainRecalls
FDA Drug Low Class III Terminated

Foradil Aerolizer (formoterol fumarate inhalation powder) 12 mcg per capsule, 12 Capsules (Blister strips of 6) per pack. For inhalation use only, Rx only, Manufactured for: Merck Sharp & Dohme Corp., a subsidiary of MERCK & CO., INC. Whitehouse Station, NJ 08889. Manufactured by: Novartis Pharma AG Basle,Via Serafino Balestra 31 Locarno, Switzerland.

Reported: June 24, 2015 Initiated: May 22, 2015 #D-1137-2015

Product Description

Foradil Aerolizer (formoterol fumarate inhalation powder) 12 mcg per capsule, 12 Capsules (Blister strips of 6) per pack. For inhalation use only, Rx only, Manufactured for: Merck Sharp & Dohme Corp., a subsidiary of MERCK & CO., INC. Whitehouse Station, NJ 08889. Manufactured by: Novartis Pharma AG Basle,Via Serafino Balestra 31 Locarno, Switzerland.

Reason for Recall

Failed Stability Specification: out of specification result obtained for the Particle Size Distribution test during stability testing.

Details

Units Affected
19,658 packs
Distribution
NJ via 1 distributor
Location
Suffern, NY

Frequently Asked Questions

What product was recalled?
Foradil Aerolizer (formoterol fumarate inhalation powder) 12 mcg per capsule, 12 Capsules (Blister strips of 6) per pack. For inhalation use only, Rx only, Manufactured for: Merck Sharp & Dohme Corp., a subsidiary of MERCK & CO., INC. Whitehouse Station, NJ 08889. Manufactured by: Novartis Pharma AG Basle,Via Serafino Balestra 31 Locarno, Switzerland.. Recalled by Novartis Pharmaceuticals Corp.. Units affected: 19,658 packs.
Why was this product recalled?
Failed Stability Specification: out of specification result obtained for the Particle Size Distribution test during stability testing.
Which agency issued this recall?
This recall was issued by the FDA Drug on June 24, 2015. Severity: Low. Recall number: D-1137-2015.