Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
FDA Recall Z-0319-2024 · Posted 2023-11-16
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Recalling FirmPhilips North America
Recall StatusOpen, Classified
Product CodeJAK
Date Initiated2023-10-09
Product Quantity1 unit
Reason for Recall
This recall is part of a 2-issue recall for the same system. When using the IVC needle position button, on the IVC control box during a series of scans, the plan box may not move to the desired needle position. This issue could result in the gantry moving to a location the operator does not expect. If this occurs, it presents a risk that the scan could occur at an incorrect location, or that the unintended motion of the gantry could cause a collision with the user or needle.
The other part of the recall involves a software crash when the CCT foot pedal is activated (as described in RES ID93363).
Firm Action
An URGENT Medical Device Correction notification letter dated 10/9/23 was sent to customers.
Actions that should be taken by the customer / user in order to prevent risks for patients or users Below are short-term precautions to take until the permanent solution is installed.
Remain vigilant and confirm gantry position during procedures. Review the Emergency Stop Procedure and Collision Prevention Guidelines provided in Section 6: Working with Specialized Exams of the IFU.
Actions planned by Philips to correct the problem
Philips will contact you to schedule a time for a Philips Field Service Engineer (FSE) to visit your site and install the software update (FCO 72800805) to resolve the issue.
Please be assured that maintaining a high level of safety and quality is our highest priority. If you need any further information or support concerning this issue, please contact the Customer Care Solutions Center (1-800-722-9377).
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the state of MN.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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