Recall Z-2374-2025 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
Philips Ultrasound, Inc
L12-4 Lumify Transducer Probe
| Date | Aug 22, 2025 (initiated Jul 3, 2025) |
| Status | Open, Classified |
| Reason | To provide clarification and labelling to define the useful life of ultrasound transducers in the field. |
| Root cause | Device Design |
| Action | An URGENT Medical Device Correction Notice, dated 7/3/25, was mailed to consignees. This notice instructs consignees to locate all Philips Ultrasound transducers in their facility and enter their serial numbers into https://www.transducer.philips.com to obtain the manufacturing certificate for each of their devices. This certificate should be retained with its system documentation. Using the manufacturing certificate consignees are to calculate the useful life of their device. The expected useful life for Transesophageal transducers, X-Matrix transducers, and Lumify transducers is 5 years; The |
| Quantity | 171,322 units |
| Distribution | US Nationwide distribution. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K152899 | Philips Lumify Diagnostic Ultrasound System Philips Healthcare, Inc., Oct 30, 2015 |
| K162549 | Lumify Ultrasound System Philips Health Care, Oct 3, 2016 |
| K192226 | Lumify Diagnostic Ultrasound System Philips Health Care, Sep 6, 2019 |
| K201012 | EPIQ Diagnostic Ultrasound System Series, Affiniti Diagnostic Ultrasound System Series, CX50 Diagnostic Ultrasound Syste Philips Ultrasound, Inc., May 1, 2020 |
| K203406 | Lumify Diagnostic Ultrasound System Philips Ultrasound, Inc., Feb 23, 2021 |