FDA Device recall Z-2383-2025
mC12-3 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of mC12-3 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-2383-2025 |
| 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
mC12-3 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605495721; UDI: (01)00884838093935(21)F0FKJ7, 010088483809393521F0FRHZ, (01)00884838093935(21)B3XYRY, (01)…Model No. 989605495721; UDI: (01)00884838093935(21)F0FKJ7, 010088483809393521F0FRHZ, (01)00884838093935(21)B3XYRY, (01)00884838093935(21)B4161X, (01)00884838093935(21)F07K8J, (01)00884838093935(21)F0JTY0, (01)00884838093935(21)F04YTZ, (01)00884838093935(21)F0550K, (01)00884838093935(21)F094Y9, (01)00884838093935(21)F0GJC9, (01)00884838093935(21)B3XZRM, (01)00884838093935(21)F0KC6Y, (01)00884838093935(21)F0HP38, (01)00884838093935(21)F0F164, (01)00884838093935(21)F0KND1, (01)00884838093935(21)F04YV6, 010088483809393521B3Y0KC, (01)00884838093935(21)F0JZQ6, (01)00884838093935(21)F0JZQ7, (01)00884838093935(21)B3XZ5Q, (01)00884838093935(21)F07WW2, (01)00884838093935(21)F07WW9, (01)00884838093935(21)F07WWF, (01)00884838093935(21)F07WWJ, (01)00884838093935(21)F07WWL, (01)00884838093935(21)F07WWN, (01)00884838093935(21)F07WWP, (01)00884838093935(21)F07WWQ, (01)00884838093935(21)F07ZZ0, (01)00884838093935(21)F081V3, (01)00884838093935(21)F08H3V, (01)00884838093935(21)F05FK6, (01)00884838093935( |
|---|
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-2383-2025%22
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