Product Wiki · Recalls · Health Canada — Medical Devices

Axiom Artis and Artis Zee Devices (2014-05-14) — recall 51959

Health Canada — Medical Devices · Canada · 2014-06-05 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
51959
Date of alert
2014-06-05
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: A problem can occur, if by mistake the wireless footswitch gets disconnected from the loading station due to an unintentional pull of the plug connection. In this case, it is necessary to loosen the interlocking mechanism. However, if this does not happen properly, the plug can become damaged. As a consequence, this could have the implication that the wireless footswitch can no longer be charged.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/axiom-artis-and-artis-zee-devi

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