Recall Z-2050-2025 ยท ITX Transducer, Ultrasonic, Diagnostic
Philips Ultrasound, Inc
Philips C5-2 Transducer.
| Date | Jul 2, 2025 (initiated May 28, 2025) |
| Status | Open, Classified |
| Reason | Ultrasound transducer devices were refurbished beyond their useful life. |
| Root cause | Process control |
| Action | An URGENT Medical Device Recall notification dated 5/28/25 was mailed to consignees. The notification informs consignees that Philips Ultrasound will be replacing transducers that were refurbished beyond their useful life with a new transducer. Consignees may continue to use affected devices while awaiting replacement; consignees should use devices in accordance with their intended use and per the instructions provided int he User Manual. Users should perform visual inspection and electrical safety testing as indicated in the User Manual; if a device does not pass inspection, it should be remo |
| Quantity | 5,230 units |
| Distribution | Domestic: Nationwide Distribution; Foreign: Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Latvia, Lebanon, Luxembourg, |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K030455 | BORIS PLATFORM DIAGNOSTIC ULTRASOUND SYSTEM Philips Ultrasound, Inc., Mar 13, 2003 |
| K043535 | HD11 DIAGNOSTIC ULTRASOUND SYSTEM Philips Ultrasound, Inc., Jan 6, 2005 |
| K081661 | HD15 DIAGNOSTIC ULTRASOUND SYSTEM Philips Ultrasound, Inc., Jun 24, 2008 |
| K120321 | CLEARVUE 350/550 DIAGNOSTIC ULTRASOUND SYSTEM Philips Health Care, Feb 17, 2012 |
| K133833 | NUVIS DIAGNOSTIC ULTRASOUND SYSTEM Philips Ultrasound, Inc., Jan 17, 2014 |