FDA Device recall Z-2373-2025
L12-4 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 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-2373-2025 |
| 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 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605430652, 989605409562, 989605427122, 989605463401, 989605430651, 989605442161, 989605418963, 98960538785…Model No. 989605430652, 989605409562, 989605427122, 989605463401, 989605430651, 989605442161, 989605418963, 989605387852, 989605418701, 989605387081, 989605412042, 989605451171, 989605463401; UDI: (01)00884838061484(21)B1X9ZR, (01)00884838061484(21)B2Y9KT, (01)00884838061484(21)B30VBJ, (01)00884838061484(21)F001VD, (01)00884838061583(21)B1XBZR, (01)00884838061644(21)B1NM93, (01)00884838061644(21)B1NM97, (01)00884838061644(21)B1PKN3, (01)00884838061644(21)B1PKNX, (01)00884838061644(21)B1QC9Q, (01)00884838061644(21)B2C3WV, (01)00884838061644(21)B36X3B, (01)00884838061644(21)B3G91R, (01)04719873000043(21)B3Q2BY, (01)04719873000043(21)F0FFRZ, (01)04719873000043(21)F0HHBM, (01)04719873000043(21)F0JKV3, 010471987300004321B24KV9, (01)00884838067882(21)B32NGP, (01)00884838067882(21)B3FP9D, (01)00884838067882(21)B27L19, (01)00884838067882(21)B2D56Y, (01)00884838061491(21)B2JT8X, (01)00884838067882(21)B1N3XG, (01)00884838067882(21)B1N3Z3, (01)00884838067882(21)B2PT8J, (01)00884838067882(21)B2THV |
|---|
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-2373-2025%22
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