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LMA Mucosal Atomization Devices
- Starting date:
- October 31, 2016
- Posting date:
- November 18, 2016
- 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-61104
Reason
Teleflex is recalling these products as they may produce a straight stream instead of a fully atomized plume of medication. This may result in inadequate topical anesthesia which may lead to some discomfort, further attempts to deliver topical anesthesia, or the use of alternative methods of anesthesia.
Affected products
LMA Mucosal Atomization Devices
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
- MAD600
- MAD700
- MAD720
Companies
- Manufacturer
-
Wolfe Tory Medical Inc.
18 - 79 West 4500 Ave. South
Salt Lake City
84107
Utah
UNITED STATES