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Cardiovit AT-102 Plus
- Starting date:
- January 9, 2017
- Posting date:
- February 9, 2017
- 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-62134
Reason
Patient data mix-up may happen when the setting of "Manual Send" and "Automatic Erase After Send" is chosen for the data transmission.
Affected products
Cardiovit AT-102 Plus
Lot or serial number
- 1.21
- 1.22
- 1.23
Model or catalog number
- 0.075000
Companies
- Manufacturer
-
Schiller AG
Altgasse 68
Baar
6341
SWITZERLAND