FDA Device recall Z-2356-2025
C6-3 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of C6-3 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-2356-2025 |
| 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
C6-3 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605359593, 989605387371, 989605359594, 989605359591; UDI: (01)00884838067950(21)B20N4N, (01)00884838067950…Model No. 989605359593, 989605387371, 989605359594, 989605359591; UDI: (01)00884838067950(21)B20N4N, (01)00884838067950(21)B1WR9H, (01)00884838067950(21)B1RGN0, (01)00884838067950(21)B1MTT4, (01)00884838067950(21)B1N3C4, (01)00884838087170(21)B27LPZ, (01)00884838087170(21)B3W5CM, (01)00884838067950(21)B24KL3, (01)00884838067950(21)B1MTT5, (01)00884838087170(21)B27LQ2; Serial No. B20N4N, B1WR9H, B1RGN0, B1MTT4, B16QBM, B1N3C4, B27LPZ, 03DG3C, B3W5CM, B2ZN6B, B19M3K, B2TJFT, B35M7F, B24KL3, B1MTT5, B32P04, B35MC6, B27LQ2. |
|---|
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-2356-2025%22
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