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DUODENOVIDEOSCOPE (2016-01-21)
- Starting date:
- January 21, 2016
- Posting date:
- February 8, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-57050
Affected Products
A. DUODENOVIDEOSCOPE
Reason
Olympus is conducting a corrective action of all TJF-Q180V duodenoscopes in order to replace the forceps elevator mechanism. Olympus has also updated the existing TJF-Q180V operation manual and reprocessing manual with a new operation manual and a new reprocessing manual.
Affected products
A. DUODENOVIDEOSCOPE
Lot or serial number
All lots.
Model or catalog number
TJF-Q180V
Companies
- Manufacturer
-
Olympus Medical Systems Corp.
2951 Ishikawa-cho
Hachioji-shi, Tokyo
192-8507
JAPAN