FDA Device recall Z-2384-2025
mC7-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of mC7-2 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-2384-2025 |
| 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
mC7-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605486021; UDI: (01)00884838088160(21)F0H6NW, (01)00884838088160(21)B35HXY, (01)00884838088160(21)B3HWCY,…Model No. 989605486021; UDI: (01)00884838088160(21)F0H6NW, (01)00884838088160(21)B35HXY, (01)00884838088160(21)B3HWCY, (01)00884838088160(21)B3WVGJ, (01)00884838088160(21)B3WW12, (01)00884838088160(21)B3WW13, (01)00884838088160(21)F0JRVZ, (01)00884838088160(21)B40Q3K, (01)00884838088160(21)F04Q9N, (01)00884838088160(21)F09LNY, (01)00884838088160(21)B40GFT, (01)00884838088160(21)B40HCB, (01)00884838088160(21)B3Y5LX, (01)00884838088160(21)F0D2Q3, (01)00884838088160(21)F0F7Z8, (01)00884838088160(21)F0F7Z9, (01)00884838088160(21)F0FGNZ, (01)00884838088160(21)F0FGP7, (01)00884838088160(21)F0F627, (01)00884838088160(21)F04QB2, (01)00884838088160(21)B39RCM, (01)00884838088160(21)B3XFVY, (01)00884838088160(21)B3YRZK, (01)00884838088160(21)B3Y3Z9, (01)00884838088160(21)F0H6P0, (01)00884838088160(21)F0HBW0, (01)00884838088160(21)B35CT2, (01)00884838088160(21)B3HLT9, (01)00884838088160(21)B35CWP, (01)00884838088160(21)B3W4VD, (01)00884838088160(21)B3XWND, (01)00884838088160(21)B3XXY8, (01)0088483 |
|---|
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-2384-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.