Ambu aView 2 Advance
Brand(s)
Last updated
Summary
Product
Ambu aView 2 Advance
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products | Lot or serial number | Model or catalog number |
---|---|---|
Ambu aview 2 Advance | All lots. | 405011000 405011000US1 405011000US2 |
Issue
Ambu has received information on two incidents where Ambu® aView™ 2 Advance caught fire when mounted on the vesa holder of the aCart™ compact, due to incorrect length screws used penetrating the lithium-ion battery of the device. Investigations have identified that the fire hazard was a direct consequence of a battery short-circuit, which, in turn, was triggered by the use of excessively long screws to mount the device. There is no instruction for mounting in the IFU accompanying the device.
Recall Start Date: November 18, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
Ambu A/S
Baltorpbakken 13, Ballerup, Denmark, 2750
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74680
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