Product Wiki · Recalls · Health Canada — Medical Devices

Allura Xper FD10, FD20, FD10/10, and FD20/10 (2018-06-12) — recall 58258

Health Canada — Medical Devices · Canada · 2018-08-17 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
58258
Date of alert
2018-08-17
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The first time an operator selects a new procedure type during a single examination, the shutter position resets to the open position for the new procedure type. If the shutters had previously been changed during the examination, that setting is not retained after the first time the procedure type is changed during a single examination.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10-fd20-fd1010-a

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