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LMA MAD Nasal Intranasal Mucosal Atomization Devices
- Starting date:
- April 18, 2017
- Posting date:
- June 7, 2017
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-63498
Reason
Teleflex Medical is contacting customers that received the products referenced in this recall because the instructions for use (IFU) have been revised to include the following statement "for use with drugs approved for intranasal delivery".
Affected products
LMA MAD Nasal Intranasal Mucosal Atomization Devices
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
MAD100
MAD110
MAD130
MAD140
MAD300
Companies
- Manufacturer
-
Teleflex Medical
2917 Weck Drive
Research Triangle Park
27709
North Carolina
UNITED STATES