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Navios Products
- Starting date:
- December 17, 2012
- Posting date:
- December 17, 2012
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices, Electrical Hazard, Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-16837
Recalled Products
- Navios 6 Colours / 2 Lasers
- Navios 8 Colours / 2 Lasers
- Navios 10 Colours / 3 Lasers
Reason
An internal wiring problem in certain Navios reagent carts that may result in a severe shock hazard and instrument failure or shut down. During manufacture the compressor cable assembly may have been installed in a configuration that would allow the wiring to come into contact with the compressor frame during operation.
Affected products
A. Navios 6 Colours / 2 Lasers
Lot or serial number
Lesser than and not equal to # AU50137.
Model or catalog number
A52101
Companies
- Manufacturer
- Beckman Coulter Inc.
B. Navios 8 Colours / 2 Lasers
Lot or serial number
Lesser than and not equal to # AU50014.
Model or catalog number
A52102
Companies
- Manufacturer
- Beckman Coulter Inc.
C. Navios 10 Colours / 3 Lasers
Lot or serial number
Lesser than and not equal to # AU45311.
Model or catalog number
A52103
Companies
- Manufacturer
- Beckman Coulter Inc.