Z-1673-2026
Class II · Ongoing
- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 20260303
- Firm location
- Best, Netherlands
Product description
Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
Reason for recall
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Data sourced from openFDA. This site is unofficial and independent of the FDA.