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9601 Documentation Cart with Articulating Arm
- Starting date:
- June 16, 2009
- Posting date:
- January 7, 2013
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public (GP), Healthcare Professionals, Hospitals
- Identification number:
- RA-16495
Recalled Products
A. 9601 Documentation Cart with Articulating Arm
Reason
The articulating arm of the 9601F Cart may fall off during manipulation.
Affected products
9601 Documentation Cart with Articulating Arm
Lot or serial number
N/A
Model or catalog number
9601F
Companies
- Manufacturer
- Karl Storz Endoscopy - America (KSEA)