PHILIPS HOME HEALTHCARE SOLUTION: Medical Device Recall in 2021 - (Recall #: Z-0727-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system

Product Classification:

Class II

Date Initiated: December 8, 2020

Date Posted: February 3, 2021

Recall Number: Z-0727-2021

Event ID: 87039

Reason for Recall:

After the user selects the Lock-in command, the kV and mA values are not locked immediately and can adjust if the collimator shutter position is changed directly after the Lock-in command.

Status: Terminated

Product Quantity: 91

Code Information:

Pending

Distribution Pattern:

Nationwide

Voluntary or Mandated:

FDA Mandated