Cambridge, MA, United States
PHILIPS HOME HEALTHCARE SOLUTION recalls
1 recall recorded since 2018, most recently on 8 December 2020. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 8 December 2020
- Terminated
- 21 June 2024
- Reason
- 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.
- Distribution
- Nationwide
- Initiated
- FDA Mandated
- Recall number
- Z-0727-2021
- ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.