RecallRadar

FDA Device recall Z-2217-2024

NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2

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

AgencyFDA Device
Recall numberZ-2217-2024
ClassificationClass II
Statusongoing
Initiated2024-05-06
Published2024-07-03
Last updated2026-09-13 11:57 UTC
CompanyNovasignal
DistributionUS

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

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.