Lma Mucosal Atomization Devices

LMA Mucosal Atomization Device Recall LMA Mucosal Atomization Devices are being recalled across Canada due to a defect that can cause the spray mechanism to malfunction or separate during use. The devices are medical instruments used to deliver medication as a spray to the mouth and throat. This recall affects all LMA Mucosal Atomization Devices currently in distribution in Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-11-18

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fe2d4efd-b2a0-4dbe-ba95-f03b0590245e