FDA Device recall Z-2380-2025
L18-5 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L18-5 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-2380-2025 |
| 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
L18-5 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605409582, 989605438531; UDI: (01)00884838061590(21)B211XD, (01)00884838061590(21)B29X8C, (01)008848380615…Model No. 989605409582, 989605438531; UDI: (01)00884838061590(21)B211XD, (01)00884838061590(21)B29X8C, (01)00884838061590(21)B2VJ24, (01)00884838061590(21)F010Y2, (01)00884838061590(21)F04JYB, (01)00884838061590(21)F06LTM, 010088483806159021F024QP, (01)00884838061590(21)B23T88, (01)00884838061590(21)B2KLW4, (01)00884838061590(21)B2LL93, (01)00884838061590(21)F0DJP0, (01)00884838061590(21)B1ZQTL, (01)00884838061590(21)B2ZCHP, (01)00884838061590(21)B1NXX9, (01)00884838061590(21)B1QBQ0, (01)00884838061590(21)F01CK2, (01)00884838061590(21)B2T427, (01)00884838061590(21)B2X16F, (01)00884838061590(21)F08GP4, (01)00884838061590(21)B1RYJ0, (01)00884838061590(21)B26Q0R, (01)00884838061590(21)B285X3, (01)00884838061590(21)B2860F, (01)00884838061590(21)B286JG, (01)00884838061590(21)B28C28, (01)00884838061590(21)B28MPM, (01)00884838061590(21)B28641, (01)00884838061590(21)F09LKN, (01)00884838061590(21)B1P4DQ, (01)00884838061590(21)B2XFLV, (01)00884838061590(21)F0C64G, (01)00884838061590(21)B1ML3D, ( |
|---|
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-2380-2025%22
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