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ENCOR MR FOOTSWITCH (2016-03-30)
- Starting date:
- March 30, 2016
- Posting date:
- April 7, 2016
- 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-57848
Affected products
A. ENCOR MR FOOTSWITCH
Reason
Bard is recalling specific product code / serial number combinations because the product labeling indicates that the enclosed footswitch is the MRI compatible footswitch (product code fsencormr) however, the actual provided footswitch is the standard footswitch (product code fsencor01).
Affected products
A. ENCOR MR FOOTSWITCH
Lot or serial number
3856
Model or catalog number
FSENCORMR
Companies
- Manufacturer
-
SENORX INC
1625 WEST 3RD STREET
TEMPE
85281
Arizona
UNITED STATES