This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
LMA MAD Nasal Intranasal Mucosal Atomization Device
- Starting date:
- October 27, 2016
- Posting date:
- November 14, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type I
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-61016
Affected Products
Reason
Teleflex is recalling these products as they may not deliver a fully atomized fine spray of medication. The failure of the device to deliver an atomized fine spray may impair the effectiveness of the medication with which it is used.
Affected products
LMA MAD Nasal Intranasal Mucosal Atomization Device
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
MAD100
MAD130
MAD140
MAD300
Companies
- Manufacturer
-
Teleflex Medical Canada Inc
500 Hood Road, Suite 310
Markham
L3R 9Z3
CANADA