FDA Device recall Z-2374-2025
L12-4 Lumify Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of L12-4 Lumify 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-2374-2025 |
| 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
L12-4 Lumify Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605434813, 989605451171, 989605434812, 989605477121, 989605434811; UDI: (01)00884838085169(21)B3GM1J, (01…Model No. 989605434813, 989605451171, 989605434812, 989605477121, 989605434811; UDI: (01)00884838085169(21)B3GM1J, (01)00884838072305(21)B21GN4, (01)00884838085169(21)F07MZ5, (01)00884838068759(21)B21Z05, (01)00884838085169(21)B35YH3, (01)00884838085169(21)F0FG0Y, (01)00884838086586(21)B2C7QM, (01)00884838085169(21)B25WBT, (01)00884838085169(21)F01RBW, (01)00884838085169(21)F0CJ0M, (01)00884838085169(21)F0KW5F, (01)00884838085169(21)F00CDB, (01)00884838085169(21)F0DC9D, (01)00884838085169(21)F0DCLR, (01)00884838085169(21)F0DDF7, (01)00884838085169(21)F0DF57, (01)00884838085169(21)F0DF5D, (01)00884838085169(21)F02WK6, (01)00884838085169(21)F08PRN, (01)00884838085169(21)B2J24P, (01)00884838086586(21)B2C7PX, 010088483808516921B27DHQ, 010088483808516921B2J2CN, (01)00884838085169(21)F0F0B8, (01)00884838085169(21)F0FCP7, (01)00884838085169(21)B27CFY, (01)00884838085169(21)B27F3B, (01)00884838085169(21)F066CP, (01)00884838085169(21)F00PYH, (01)00884838085169(21)F0KTDZ, (01)00884838085169(21) |
|---|
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-2374-2025%22
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