FDA Device recall Z-2217-2024
NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2
- FDA Device
- Class II
- ongoing
- Published 2024-07-03
On 2024-07-03 the FDA classified a Class II recall of NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2 by Novasignal, citing due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2217-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-06 |
| Published | 2024-07-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Novasignal |
| Distribution | US |
Product
NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2
Reason
Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.
Identifiers
| code_info | UDI: 00850681007405/Serial Numbers: 21092746 21122802 21122803 21092748 21092749 21122804 21123066 23063826 2207438…UDI: 00850681007405/Serial Numbers: 21092746 21122802 21122803 21092748 21092749 21122804 21123066 23063826 22074381 23063828 22033706 22064206 22074380 21092747 22113115 23063825 21122805 21082646 23063856 23104174 21123068 22103022 22064204 22064205 21123067 22074378 22074379 23033578 |
|---|
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-2217-2024%22
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