FDA Device recall Z-2369-2025
eL18-4 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of eL18-4 Transducer Probe by Philips Ultrasound, citing to provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2369-2025 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2025-07-03 |
| Published | 2025-09-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Ultrasound |
| Distribution | US |
Product
eL18-4 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605431531, 989605456291, 989605391092, 989605412062, 989605409562; UDI: (01)00884838070806(21)B3DVRN, (01)…Model No. 989605431531, 989605456291, 989605391092, 989605412062, 989605409562; UDI: (01)00884838070806(21)B3DVRN, (01)00884838070806(21)B3NTCY, (01)00884838070806(21)F05K3C, (01)00884838070813(21)B3J1RW, (01)00884838070813(21)B3KZY9, (01)00884838070813(21)F04T5F, (01)00884838070813(21)F0952L, (01)00884838070813(21)F0DYQG, (01)00884838070813(21)F0KLBR, 010088483807080621F01T01, (01)00884838070813(21)F0LWXK, (01)00884838070813(21)F0GMZ9, (01)00884838070806(21)F0JYQZ, (01)00884838070813(21)F0GN24, 010088483807081321F0FT37, 010088483807081321F0GD1D, 010088483807081321F0GDDJ, (01)00884838070806(21)B39ZR0, (01)00884838070806(21)B3BYRP, (01)00884838070806(21)B3KRZF, (01)00884838070813(21)F0LV0Z, (01)00884838070806(21)B3KRZG, (01)00884838070806(21)F04836, (01)00884838070806(21)F04N2M, (01)00884838070813(21)B3JQW5, (01)00884838070813(21)B3VGVT, (01)00884838070806(21)F03QB1, (01)00884838070806(21)F03XVR, (01)00884838070813(21)F089C4, (01)00884838070806(21)F0GTGK, (01)00884838070806(21)F0LDQ9, ( |
|---|
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-2369-2025%22
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