FDA Device recall Z-2403-2025
V6-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of V6-2 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-2403-2025 |
| 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
V6-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605415042, 989605437982, 989605438461, 989605357563, 989605357561, 989605387201, 989605415041, 98960544901…Model No. 989605415042, 989605437982, 989605438461, 989605357563, 989605357561, 989605387201, 989605415041, 989605449011, 989605395631, 989605454101; UDI: (01)00884838061460(21)B1VJQF, (01)00884838061460(21)B2RL4B, (01)00884838061651(21)B20WVG, (01)00884838061651(21)B28DGB, (01)00884838061651(21)B304XN, (01)00884838061651(21)B35CH3, (01)00884838061651(21)B20WW0, (01)00884838061651(21)B1YQQ6, (01)00884838061651(21)B1XLYC, (01)00884838061651(21)B1YQZR, (01)00884838061651(21)B1P7QY, (01)00884838061651(21)B2G0CC, (01)00884838061651(21)B2LN7C, (01)00884838061651(21)B2RL6L, (01)00884838061651(21)B1P7TG, (01)00884838061651(21)B2RL9K, (01)00884838061651(21)B1P7Q8, (01)00884838061651(21)B20WM1, (01)00884838061651(21)B20WKR, (01)00884838061651(21)B1P7PJ, (01)00884838061651(21)B1XLYW, (01)00884838061651(21)B1XLZ0, (01)00884838061651(21)B2NP4F, (01)00884838061651(21)B28CZW, (01)00884838061651(21)B2LMY0, (01)00884838061798(21)B05KK0, (01)00884838061798(21)B0QV98, (01)00884838061651(21)B20X0M, (01)0 |
|---|
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-2403-2025%22
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