Philips North America: Medical Device Recall in 2024 - (Recall #: Z-1073-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:706150

Product Classification:

Class II

Date Initiated: December 15, 2023

Date Posted: February 21, 2024

Recall Number: Z-1073-2024

Event ID: 93773

Reason for Recall:

Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a previous patients radiography (RAD) images when starting the next patient scan while the previous patient image export is still processing. If the issue occurs, there is a potential for incorrect patient data to be displayed in the image. Issue 2: Detector Access point: Security vulnerability specific to the Wireless Portable Detector configuration items in Philips Support Connect (PSC). Due to this vulnerability it is possible, with physical access to the system and knowledge of specific settings, to modify and export data to removable media (example: USB)

Status: Ongoing

Product Quantity: 20 units: 16 units US; 4 units OUS

Code Information:

UDI: N/A Serial Numbers US: 4 5 6 7 8 9 11 12 13 14 17 18 61 692222229 692222254 692222263 Serial Numbers OUS: 53 56 65 692222227

Distribution Pattern:

Nationwide Foreign: Australia Germany India Italy Malaysia Panama Thailand

Voluntary or Mandated:

Voluntary: Firm initiated