Health product recall

Lumify Ultrasound System

Last updated

Summary

Product
Lumify Ultrasound System
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 catalogue number

Lumify Ultrasound System

Not applicable.

3.0

Lumify Ultrasound System

Not applicable.

LUMIFY ULTRASOUND SYSTEM

Lumify Ultrasound System

Not applicable.

4.0

Lumify Diagnostic Ultrasound System

Not applicable.

795005

Lumify Diagnostic Ultrasound System iOS

Not applicable.

795161

Lumify Diagnostic Ultrasound System iOS

Not applicable.

5.1.3

Issue

Potential issues with the Lumify Diagnostic Ultrasound System which may prevent or delay scanning functionality:

  1. 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.
  2. 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.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies
Philips Ultrasound Llc
22100 Bothell Everett Highway, Bothell, Washington, United States, 98021
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Recall date
Identification number
RA-82731

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