FDA Device recall Z-2360-2025
C9-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of C9-2 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-2360-2025 |
| 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
C9-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605391092, 989605438431, 989605418552, 989605391091, 989605412042; UDI: (01)00884838061507(21)B3G8WQ, 010…Model No. 989605391092, 989605438431, 989605418552, 989605391091, 989605412042; UDI: (01)00884838061507(21)B3G8WQ, 010088483806150721F0G8PX, (01)00884838061507(21)B25KL1, (01)00884838061507(21)B2L2LB, 010088483806150721F0FWFW, 010088483806150721F0G0CF, (01)00884838061507(21)F02CP6, (01)00884838061507(21)B26BXV, (01)00884838061507(21)B28G5L, (01)00884838061507(21)B2FG9B, (01)00884838061507(21)B3G8M5, (01)00884838061507(21)F03V2C, (01)00884838061507(21)F040X0, (01)00884838061507(21)F0G485, (01)00884838061507(21)B3NLL9, (01)00884838061507(21)F03W2J, 010088483806150721F0G524, (01)00884838061507(21)B1ZXP6, (01)00884838061507(21)F03Y53, (01)00884838061507(21)F0860Z, (01)00884838061507(21)F0JPXD, (01)00884838061507(21)B331YR, (01)00884838061507(21)F05CDM, (01)00884838061507(21)F05DYV, (01)00884838061507(21)F05VLL, 010088483806150721F0G59Y, (01)00884838061507(21)B3RFXC, (01)00884838061507(21)F03TK9, (01)00884838061507(21)B22HP1, (01)00884838061507(21)B250V0, (01)00884838061507(21)B1PL8N, (01) |
|---|
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-2360-2025%22
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