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ARJOHUNTLEIGH MAXI MOVE HANDSET (2016-05-20)
- Starting date:
- May 20, 2016
- Posting date:
- November 30, 2017
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- Healthcare Professionals, General Public, Hospitals
- Identification number:
- RA-65248
Affected products
ARJOHUNTLEIGH MAXI MOVE HANDSET
Reason
ArjoHuntleigh has been made aware from internal testing and investigative activities that the conductive ink which is necessary for the activation of the handset function did not meet predetermined durability requirements. As part of our efforts to ensure customer satisfaction and product quality and performance, ArjoHuntleigh has decided to perform a replacement of handset for the Maxi Move Floor Lifts affected by this issue, which is not expected to affect the safety of the device, but rather its durability.
Affected products
ARJOHUNTLEIGH MAXI MOVE HANDSET
Lot or serial number
More than 100 numbers, contact manufacturer.
Model or catalog number
KMC***
Companies
- Manufacturer
-
ArjoHuntleigh AB
Hans Michelsensgatan 10
Malmo
21120
SWEDEN