Philips Azurion Systems Angiographic X-ray
Recall Summary Philips is recalling Azurion Systems Angiographic X-Ray devices distributed to hospitals and laboratories in New Zealand. The devices require modification to address an unspecified safety concern. This is classified as a Class I recall, the most serious category.
- Recalling firm
- Philips New Zealand Commercial Limited
- Product
- Philips Azurion Systems Angiographic X-Ray. [Device]. Model: Philips Azurion 7 M20 Systems - system code 722079
- Reason
- The manufacturer has identified that the Float Tabletop control on the control module of Azurion systems may experience mechanical wear over time. The Float Tabletop control is located on the control module at the table-side. When the control is actuated, the table brakes disengage, allowing adjustment of the longitudinal or transverse position of the table. Over time, mechanical wear may lead to detachment, cracking, or breakage of the Float Tabletop control, which may lead to reduced availability or unavailability of longitudinal and transverse tabletop movement, as well as the formation...
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-05-19
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/0c2391d2-32e8-4ca6-bf6d-e6bb2a4c98a1