Health ProductsType I recall

Lumify Ultrasound System

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - Radiology
Product: Lumify Ultrasound System
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type I
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Products

Affected productsLot or serial numberModel or catalogue number
Lumify Ultrasound SystemNot applicable.3.0
Lumify Ultrasound SystemNot applicable.LUMIFY ULTRASOUND SYSTEM
Lumify Ultrasound SystemNot applicable.4.0
Lumify Diagnostic Ultrasound SystemNot applicable.795005
Lumify Diagnostic Ultrasound System iOSNot applicable.795161
Lumify Diagnostic Ultrasound System iOSNot applicable.5.1.3

Issue

Potential issues with the Lumify Diagnostic Ultrasound System which may prevent or delay scanning functionality: Due to a software issue, the Lumify application may not recognize a previously registered transducer and prompt for re-registration (outside of the defined criteria in the user guide) without warning prior to point of care use. Scanning functionality is prevented until the registration step has been completed; registration requires wi-fi or cellular signal access.Lumify devices used outside the hospital, such as in ambulances, aircraft, or field settings, are at greater risk due to reduced access to wi-fi/cellular. Philips has received reports that these erroneous re-registration events have prevented scanning in pre-hospital environments and delayed care to patients. These pre-hospital events occurred outside of wi-fi or cellular access. Additionally, Philips has identified that the connection between the Lumify transducer USB cable to a customer's tablet/ phone may disconnect or have an unstable connection during use which may disrupt continuous function of the device and result in a delay of care.

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