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SKINTACT MULTIFUNCTION ELECTRODE
- Starting date:
- September 21, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type I
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-60562
Affected Products
Reason
There is a risk that these electrodes will be connected with the defibrillator only with delay or not at all. This may cause a situation in which a patient who is in a life-threatening condition and requires a defibrillation shock, cannot be treated in good time.
Affected products
SKINTACT MULTIFUNCTION ELECTRODE
Lot or serial number
More than 10 lots, contact manufacturer.
Model or catalog number
DF29N
Companies
- Manufacturer
-
Leonhard Lang GmbH
Archenweg 56, Innsbruck
Tirol
6020
AUSTRIA