Utolith Lithotripter System - Probes (2020-03-16)

Autolith Lithotripter System - Probes Recall The Autolith Lithotripter System probes are being recalled across Canada due to a medical device issue. The recall is classified as Class I, which is the most serious category. This recall affects the probes used with the Autolith Lithotripter System that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-04-17
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6a1cd57e-7350-4858-aa74-46c509dff191