Lma Mad Nasal Intranasal Mucosal Atomization Device

Recall Summary The LMA MAD Nasal Intranasal Mucosal Atomization Device has been recalled in Canada because it may not deliver medication doses accurately. This device is used to spray medication into the nasal passages for absorption through the mucous membranes. The recall affects all units distributed across Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-11-14

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/997690b3-9963-4c47-a151-057590788afa