FDA Device recall Z-2399-2025
S9-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of S9-2 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-2399-2025 |
| 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
S9-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605472101, 989605400802, 989605361882; UDI: (01)00884838086609(21)B2Y9BP, (01)00884838086609(21)B3GMC1, 0…Model No. 989605472101, 989605400802, 989605361882; UDI: (01)00884838086609(21)B2Y9BP, (01)00884838086609(21)B3GMC1, 010088483808660921F0G6T9, (01)00884838086609(21)B3M9F7, (01)00884838086609(21)F088D0, (01)00884838086609(21)F08K67, (01)00884838086609(21)F08XLT, (01)00884838086609(21)F092KQ, (01)00884838086609(21)F011V7, (01)00884838086609(21)F011VC, (01)00884838086609(21)F089HB, 010088483808660921F01Q7H, (01)00884838086609(21)F02N9G, (01)00884838086609(21)B23VNV, (01)00884838086609(21)B3R9CQ, (01)00884838086609(21)B3RFQL, (01)00884838086609(21)F01QK3, (01)00884838086609(21)F04FDY, (01)00884838086609(21)F06V0P, (01)00884838086609(21)F06ZF3, (01)00884838086609(21)F0FF6Y, (01)00884838086609(21)F0FHLF, 010088483808660921F0GH6F, N/A, (01)00884838086609(21)B2R8CV, (01)00884838086609(21)F04HG7, (01)00884838086609(21)F0CM8H, (01)00884838086609(21)F08VD8, (01)00884838086609(21)F0HCFG, (01)00884838086609(21)B2Z070, (01)00884838086609(21)F06B02, (01)00884838086609(21)B32B8K, (01)00884838086609( |
|---|
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-2399-2025%22
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