FDA Device recall Z-2057-2025
Philips L9-3 Transducer
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of Philips L9-3 Transducer by Philips Ultrasound, citing ultrasound transducer devices were refurbished beyond their useful life.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2057-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-05-28 |
| Published | 2025-07-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
Philips L9-3 Transducer.
Reason
Ultrasound transducer devices were refurbished beyond their useful life.
Identifiers
| code_info | Model No. 989605353301, 989605353303, 989605387361; UDI: N/A; Serial No. B0ZTD1, 03F40C, 03923H, 0314BQ, 03712H, 033HGC…Model No. 989605353301, 989605353303, 989605387361; UDI: N/A; Serial No. B0ZTD1, 03F40C, 03923H, 0314BQ, 03712H, 033HGC, 03CJ9M, 035JY0, 03CFTH, 0399XP, 030FNL, 037R81, 02ZH61, 0358PF, 033JGV, 03FN82, 03230B, 03145Y, 02XYB3, 02XWH4, 02Z1D9, 03591C, 0359Q1, 03598Y, 035JVM, 02WVF0, 02WYT1, 03CFPG, 02XWN1, 02ZJR6, 02NV7G, 0305WC, 036XY3, 02XY9D, 03FNPD, 02ZJPH, B08PVN, 0373HX, B0NP6L, 03F364, 03922W, 02X173, 02WYQX, 02ND56, 0367GW, 0315P3, 02QMTL, 038W72, 03315L, 0358PV, 033JK7, 03128V, 032297. |
|---|
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-2057-2025%22
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