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Medisorb (2013-09-11)
- Starting date:
- September 11, 2013
- Posting date:
- October 28, 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-36441
Recalled Products
Medisorb
Reason
The multi absorber original may have a thin wall condition which may lead to small holes in the water (drain) tube. This may result in a loss of anesthetic gases, ventilation and oxygenation.
Affected products
Medisorb
Lot or serial number
Not applicable
Model or catalog number
- M1173310
Companies
- Manufacturer
-
GE Healthcare Finland OY
Kuortaneenkatu 2,
Hesinki
00510
FINLAND