FDA Device recall Z-2393-2025
S4-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of S4-2 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-2393-2025 |
| 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
S4-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605414692, 989605463421, 989605442131, 989605387731, 989605412042, 989605430222, 989605381211, 98960543065…Model No. 989605414692, 989605463421, 989605442131, 989605387731, 989605412042, 989605430222, 989605381211, 989605430652, 989605361982, 989605463421; UDI: (01)00884838067844(21)B2TH04, (01)00884838067844(21)B2TH20, (01)00884838067844(21)B2TH5R, (01)00884838067844(21)B2TH94, (01)00884838067844(21)B2TH95, (01)00884838067844(21)B2TRZG, (01)04719873000067(21)F0771Y, (01)04719873000067(21)F0K891, 010471987300006721B24RHN, (01)00884838067844(21)B2ZLWP, (01)00884838067844(21)B1N04C, (01)00884838067844(21)B1N0D2, (01)00884838067844(21)B2PXTV, (01)00884838067844(21)B2PY5Z, (01)00884838067844(21)B2TRRF, (01)00884838067844(21)B1RDM4, (01)04719873000067(21)B3TLRJ, (01)04719873000067(21)B3VZCQ, (01)00884838067844(21)B35KQ5, (01)00884838067844(21)B2ZLK8, (01)00884838067844(21)B2ZTKD, (01)00884838067844(21)B1JVZF, (01)00884838067844(21)F0G5KZ, (01)00884838067844(21)B20GTL, (01)00884838067844(21)B20QB6, 010088483806784421F0B41N, 010088483806784421F0B41W, (01)00884838067844(21)B2PTGM, (01)0088483806784 |
|---|
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-2393-2025%22
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