Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 795122
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | completed |
| Recall date | July 14, 2022 |
| Reported | January 07, 2026 |
| Recalling firm | Philips Ultrasound, LLC |
| Country / region | United States WA |
Hazard
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
Affected products
- Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201, 795231, 795232, 795234 REF: 795117, 7
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