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Bipolar Endostasis (BEST) Products
- Starting date:
- December 4, 2012
- Posting date:
- January 21, 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-16895
Recalled Products
- A. Bipolar Endostasis (BEST) Products
Reason
Unlicensed Class 2 medical devices sold into Canada.
Affected products
A. Bipolar Endostasis (BEST) Products
Lot or serial number
Not Applicable
Model or catalog number
91007
Companies
- Manufacturer
- Meditron Devices LLC