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MYNDMOVE FUNCTIONAL ELECTRICAL STIMULATOR (2015-03-10)
- Starting date:
- March 10, 2013
- Posting date:
- April 2, 2015
- 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-52769
Recalled Products
MYNDMOVE FUNCTIONAL ELECTRICAL STIMULATOR
Reason
Notification to provide information related to a known software bug that may cause a current amplitude overshoot. If encountered, the patient may receive higher current amplitude during treatment than the value that was set during the channel setup. This may affect one or more channels.
Affected products
MYNDMOVE FUNCTIONAL ELECTRICAL STIMULATOR
Lot or serial number
- 1652014C0001
- 1652014C0002
- 1652014C0003
- 1652014C0004
- 1652014C0005
- 1652014C0006
- 1652014C0007
Model or catalog number
900165
Companies
- Manufacturer
-
Myndtec Inc.,
307-2233 Argentia Road,
Mississauga,
L5N 2X7
Ontario
CANADA