FDA Device recall Z-2411-2025
X7-2 Transducer Probe
- FDA Device
- Class III
- ongoing
- Published 2025-09-03
On 2025-09-03 the FDA classified a Class III recall of X7-2 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-2411-2025 |
| 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
X7-2 Transducer Probe
Reason
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Identifiers
| code_info | Model No. 989605400812, 989605439971, 989605347573, 989605347571, 989605388121; UDI: (01)00884838061576(21)B2WXR8, (01)…Model No. 989605400812, 989605439971, 989605347573, 989605347571, 989605388121; UDI: (01)00884838061576(21)B2WXR8, (01)00884838061576(21)B2X94P, (01)00884838061576(21)B2YH00, (01)00884838061576(21)B3RTXC, (01)00884838061576(21)F01P42, (01)00884838061576(21)F04HQ8, (01)00884838061576(21)F06JLT, (01)00884838061576(21)F06M72, (01)00884838061576(21)F0FBV2, (01)00884838061576(21)F0FF0X, (01)00884838061576(21)F0GNFR, (01)00884838061576(21)F00XMF, (01)00884838061576(21)F05RCP, (01)00884838061576(21)F0GNFP, (01)00884838061576(21)B2FXP7, (01)00884838061576(21)F0DN5J, (01)00884838061576(21)B287Y8, (01)00884838061576(21)B2846C, (01)00884838061576(21)B28KC3, (01)00884838061576(21)B295K0, (01)00884838061576(21)B29731, (01)00884838061576(21)F091ZZ, (01)00884838061576(21)F0BXFT, (01)00884838061576(21)F0BXFV, (01)00884838061576(21)F0K9R8, 010088483806157621F0G8ZT, (01)00884838061576(21)B3F4KZ, (01)00884838061576(21)F04LFV, (01)00884838061576(21)B1W955, (01)00884838061576(21)F00W1B, (01)00884838061576( |
|---|
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-2411-2025%22
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