FDA Device recall Z-2379-2025
L17-5 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L17-5 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-2379-2025 |
| 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
L17-5 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 8500-1662-01, 989605366373, 989605388061, 989605366371; UDI: (01)00884838064614(21)B20XYG, (01)00884838064614…Model No. 8500-1662-01, 989605366373, 989605388061, 989605366371; UDI: (01)00884838064614(21)B20XYG, (01)00884838064614(21)B2HK04, (01)00884838064614(21)B36C77, (01)00884838064614(21)B22N5X, (01)00884838064614(21)B1YQ5T, (01)00884838064614(21)B30M34, (01)00884838064614(21)B3GX1Q, (01)00884838064614(21)B3H0X1, (01)00884838064614(21)B3P6N2, (01)00884838064614(21)B22N0X, (01)00884838064614(21)B2YF79, (01)00884838064614(21)B1XRFM, (01)00884838064614(21)B2YD0X, (01)00884838064614(21)B3BZNW, (01)00884838064614(21)B2YNKW, (01)00884838064614(21)B1QBQ1, (01)00884838064614(21)B1W401, (01)00884838064614(21)B28MR6, (01)00884838064614(21)B30M32, (01)00884838064614(21)B31CR5, (01)00884838064614(21)B3MJMX, (01)00884838064614(21)B3MK52, (01)00884838064614(21)F093DP, (01)00884838064614(21)B2JDWW, (01)00884838064614(21)B2KN10, (01)00884838064614(21)B1ZR3M, (01)00884838064614(21)B1TVHQ, (01)00884838064614(21)B2NQ1G, (01)00884838064614(21)B1VL0Y, (01)00884838064614(21)B1Q3BM, (01)00884838064614(21)B31VQ3, |
|---|
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-2379-2025%22
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