FDA Device recall Z-2364-2025
C9-4v Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of C9-4v 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-2364-2025 |
| 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
C9-4v Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605389252, 989605418972, 989605463411, 989605442141, 989605463411, 989605389251, 989605412042, 98960538709…Model No. 989605389252, 989605418972, 989605463411, 989605442141, 989605463411, 989605389251, 989605412042, 989605387091, 989605418971; UDI: (01)00884838061392(21)B1Q4CD, (01)00884838061392(21)B1YXKM, (01)00884838061392(21)B323T7, (01)00884838061392(21)F00QWD, (01)00884838061392(21)F029RH, (01)00884838067875(21)B1N3PG, (01)00884838067875(21)B1N3PZ, (01)00884838067875(21)B1N3TV, (01)00884838067875(21)B1N3W3, (01)00884838067875(21)B1N3ZJ, (01)00884838067875(21)B20M3Y, (01)00884838067875(21)B27LZD, (01)00884838067875(21)B27LZH, (01)00884838067875(21)B2TR7C, (01)00884838067875(21)B2ZMR5, (01)00884838067875(21)B32NH8, (01)00884838067875(21)B39VT0, (01)00884838067875(21)B410QW, (01)00884838067875(21)F05HKB, (01)00884838067875(21)F0JQQG, (01)04719873000050(21)B2PTCD, (01)04719873000050(21)B32PHY, 010088483806787521B3XMR5, N/A, N/A, N/A, N/A, N/A, N/A, N/A, (01)00884838067875(21)F0L3Z8, (01)00884838061392(21)B30WYR, (01)00884838067875(21)B3Z7ZM, (01)00884838061392(21)B232FN, (01)00884838061392 |
|---|
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-2364-2025%22
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