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Penumbra Coil 400 Complex Soft
- Starting date:
- July 12, 2012
- Posting date:
- September 3, 2012
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-23853
Recalled Products
A. Penumbra Coil 400 Complex Soft
Reason
This recall has been initiated because one device was distributed in Canada prior to receiving approval for sale in July 2012.
Affected products
A. Penumbra Coil 400 Complex Soft
Lot or serial number
F23204
Model or catalog number
4006C0306
Companies
- Manufacturer
- Penumbra Inc.