FDA Device recall Z-2404-2025
V9-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of V9-2 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-2404-2025 |
| 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
V9-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605466201, 989606717071, 989605492481, 989605456291; UDI: (01)00884838088573(21)B3FMNT, (01)00884838102606…Model No. 989605466201, 989606717071, 989605492481, 989605456291; UDI: (01)00884838088573(21)B3FMNT, (01)00884838102606(21)B3FLM3, (01)00884838102606(21)B411GD, (01)00884838102606(21)F053BY, (01)00884838102606(21)F0HT0R, 010088483810260621B3Y0MP, (01)00884838102606(21)F0KG9X, (01)00884838088573(21)B3FLWW, (01)00884838102606(21)F0HT11, (01)00884838102606(21)F04XCK, 010088483810260621F0FQZG, 010088483810260621F0FVH7, (01)00884838102606(21)F06PQM, (01)00884838102606(21)F06TGM, (01)00884838088573(21)B32TQN, (01)00884838102606(21)F0HJWD, (01)00884838102606(21)F0986F, (01)00884838102606(21)F07D1M, (01)00884838088573(21)B32TQZ, (01)00884838088573(21)B32TWD, (01)00884838088573(21)B32V4Y, (01)00884838102606(21)F09LH5, (01)00884838102606(21)F0JZJM, (01)00884838102606(21)F0576P, (01)00884838102606(21)F0CN2B, (01)00884838102606(21)F0F02Q, (01)00884838102606(21)F0JL42, (01)00884838088573(21)B3FLCN, (01)00884838088573(21)B3FMXB, (01)00884838088573(21)B2PYFR, (01)00884838088573(21)B2ZR1X, (01)0088483 |
|---|
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-2404-2025%22
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