FDA Device recall Z-2347-2025
3D9-3v Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of 3D9-3v 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-2347-2025 |
| 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
3D9-3v Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605387181, 989605389272, 989605395621, 989605395622, 989605409562, 989605412042, 989605412082, 9896054150…Model No. 989605387181, 989605389272, 989605395621, 989605395622, 989605409562, 989605412042, 989605412082, 989605415031, 989605415032, 989605418972, 989605437982, 989605438451, 989605440832, 989606714071, 989606717071, 989606750021, 8500-1715-01; UDI: Unique Device Identifier (UDI), (01)00884838061545(21)B3HM2J, (01)00884838061545(21)B3FH50, 010088483806154521F0G00P, 010088483806154521F0G1J2, (01)00884838061545(21)B2LN6D, (01)00884838061545(21)B2NP6J, (01)00884838061545(21)F03YG9, (01)00884838061545(21)F03YMT, (01)00884838061545(21)F0JNY1, (01)00884838061545(21)F0JR9Z, (01)00884838061545(21)B2ZVMM, (01)00884838061545(21)F05MPP, (01)00884838061545(21)F0D8T6, (01)00884838061545(21)F0KF3X, (01)00884838061545(21)F0L24T, (01)00884838061545(21)F0L31F, (01)00884838061545(21)F0L31J, (01)00884838061545(21)F0L31N, 010088483806154521F0GBLQ, 010088483806154521F0GBLW, (01)00884838061545(21)F0K8CZ, (01)00884838061545(21)F0HM7P, (01)00884838061545(21)B286JT, (01)00884838061545(21)F0LLBD, (01)008848 |
|---|
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-2347-2025%22
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