NovaGuide 2 Traditional Ultrasound — Class II medical device recall Z-2217-2024
Ongoing recall by NovaSignal Corp., reported 2024-07-03, distributed nationwide. Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, elec
| Recall number | Z-2217-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | NovaSignal Corp., Los Angeles, CA, United States |
| Recall initiated | 2024-05-06 |
| Classified | 2024-06-27 |
| Reported by FDA | 2024-07-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 28 systems |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00850681007405 |
| Serial numbers | 21082646, 21092746, 21092747, 21092748, 21092749, 21122802, 21122803, 21122804, 21122805, 21123066, 21123067, 21123068, 22033706, 22064204, 22064205, 22064206, 22074378, 22074379, 22074380, 22074381, 22103022, 22113115, 23033578, 23063825, 23063826 and 3 more |
| Model numbers | NSC-TCDNG2 |
Product
NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2
Reason for recall
Due to inadvertently disconnecting grounding cable of ultrasound system could result in electrical shock, electrical interference and/or equipment malfunction.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2217-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.