Med-Rx Epidural Anesthesia Kit (2018-08-09)
- Starting date:
- August 9, 2018
- Posting date:
- September 7, 2018
- 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-67692
Affected products
Med-Rx Epidural Anesthesia Kit
Reason
The Perifix Catheter Connector component may not remain closed during use and in some cases leakage or disconnection of the catheters has been observed. The recall is being executed as a correction and not a product removal.
Affected products
Med-Rx Epidural Anesthesia Kit
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
- 80-8014
- 80-8018
- 80-8040
- 80-8050
- 80-8055
- 80-8057
- 80-8060N
- 80-8061
- 80-8083
- 80-8087
- 80-8104
- 80-8106
- 80-8107
- 80-8109
- 80-8110
- 80-8111
- 80-8115
- 80-8116
- 80-8117
- 80-8118
- 80-8119
- 80-8123
- 80-8125
- 80-8128
- 80-8129
- 80-8133
- 80-8134
- 80-8135
- 80-8136
- 80-8142
- 80-8144
- 80-8149
- 80-8150
Companies
- Manufacturer
-
Canadian Hospital Specialties Ltd.
2810 Coventry Road
Oakville
L6H 6R1
Ontario
CANADA