FDA Device recall Z-1554-2025
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System by Philips North America, citing potential for collimator to fall as a result of incorrect installation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1554-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-03-10 |
| Published | 2025-04-23 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Reason
Potential for collimator to fall as a result of incorrect installation.
Identifiers
| code_info | REF 712214; UDI: (01)00884838064751(21); Serial No. SN170009, SN170010, SN180072, SN180020 200037, SN160061, SN180075, 200089, SN180045, SN160096. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1554-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.