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GE Systems Products
- Starting date:
- January 3, 2013
- Posting date:
- February 4, 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, Healthcare Professionals, Hospitals
- Identification number:
- RA-20311
Recalled Products
- Ventri Dual Detector Cardiac Gamma Camera Nuclear Imaging System
- GE Discovery NM 530C System
Reason
During a patient unload following a scan the patient's fingers may be pinched between the moving cradle edge and the stationary base of the table while the table is moving outward automatically.
Affected products
A. Ventri Dual Detector Cardiac Gamma Camera Nuclear Imaging System
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
H3000ZF
Companies
- Manufacturer
- GE Systems
B. GE Discovery NM 530C System
Lot or serial number
More than 10 numbers, contact manufacturer.
Model or catalog number
S8000RA
Companies
- Manufacturer
- GE Systems