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Motomed Products
- Starting date:
- January 7, 2013
- Posting date:
- February 4, 2013
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Labelling and Packaging
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-17213
Recalled Products
- Motomed Viva1
- Motomed Viva2
- Motomed Gracile
- Motomed Letto2
Reason
Device does not have a medical device licence.
Affected products
A. Motomed Viva1
Lot or serial number
Non-applicable
Model or catalog number
Motomed Viva1
Companies
- Manufacturer
- Reck-Technic GMBH and Co.
B. Motomed Viva2
Lot or serial number
Non-Applicable
Model or catalog number
Motomed Viva2
Companies
- Manufacturer
- Reck-Technic GMBH and Co.
C. Motomed Gracile
Lot or serial number
Non-Applicable
Model or catalog number
Motomed Gracile
Companies
- Manufacturer
- Reck-Technic GMBH and Co.
D. Motomed Letto2
Lot or serial number
Non-Applicable
Model or catalog number
Motomed Letto2
Companies
- Manufacturer
- Reck-Technic GMBH and Co.