FDA Device recall Z-2414-2025
XL14-3 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of XL14-3 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-2414-2025 |
| 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
XL14-3 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605409251, 989605492481; UDI: (01)00884838074613(21)B372N5, (01)00884838074613(21)F02DPY, (01)008848380746…Model No. 989605409251, 989605492481; UDI: (01)00884838074613(21)B372N5, (01)00884838074613(21)F02DPY, (01)00884838074613(21)B3MY7N, (01)00884838074613(21)B3823F, (01)00884838074613(21)B3823J, 010088483807461321F026YH, (01)00884838074613(21)F03KJH, (01)00884838074613(21)F03G0Y, (01)00884838074613(21)F03MFH, (01)00884838074613(21)F03MFL, (01)00884838074613(21)F03MFN, (01)00884838074613(21)F09RZ3, (01)00884838074613(21)F07HBJ, (01)00884838074613(21)F0HDCN, (01)00884838074613(21)B3KTRR, (01)00884838074613(21)B33MYL, (01)00884838074613(21)B2DYZ8, (01)00884838074613(21)F009PY, (01)00884838074613(21)B371ZC, (01)00884838074613(21)F02RRD, (01)00884838074613(21)B3VBPY, (01)00884838074613(21)F03MFP, 010088483807461321F01X0L, (01)00884838074613(21)F06420, (01)00884838074613(21)F06421, (01)00884838074613(21)B2K24Z, (01)00884838074613(21)F01KYL, (01)00884838074613(21)F03171, (01)00884838074613(21)F07HBC, (01)00884838074613(21)F031BB, (01)00884838074613(21)F0B6ZT, (01)00884838074613(21)F0BP2P, (01)0 |
|---|
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-2414-2025%22
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