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Terumo Advanced Perfusion System 1 (Roller Pump Occlusion Malfunctions)
- Starting date:
- December 14, 2012
- Posting date:
- January 7, 2013
- 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-16767
Recalled Products
- Terumo Advanced Perfusion System 1
Reason
Terumo Cardiovascular Systems has received reports of various roller pump occlusion malfunctions that could result in the inability to use the pump and would then require replacement with back-up equipment. Occlusion malfunctions include stiff/difficult to adjust occlusion, loss of occlusion setting, unequal roller-to-roller occlusion and inability to adjust the occlusion.
Affected products
A. Terumo Advanced Perfusion System 1
Lot or serial number
More than 10 Numbers, Contact manufacturer
Model or catalog number
801763
Companies
- Manufacturer
- Terumo Cardiovascular Systems Corp.