Data Foundry

Medical device recalls 2024

NovaGuide 2 Intelligent Ultrasound — Class II medical device recall Z-2216-2024

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 numberZ-2216-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmNovaSignal Corp., Los Angeles, CA, United States
Recall initiated2024-05-06
Classified2024-06-27
Reported by FDA2024-07-03
DistributedNationwide (US)
Countries outside the USCA
Quantity45 systems
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00850681007399, 00850681007481
Serial numbers21041631, 21041632, 21041633, 21051651, 21081931, 21081932, 21081933, 21091951, 21091952, 21102756, 21102757, 21102759, 21102760, 21122796, 21122798, 21122799, 21122801, 22023447, 22033466, 22043986, 22064207, 22064208, 22064209, 22064210, 22064212 and 20 more
Model numbersNSC-NVGSYS2, NSC-NVGSYS2-CA

Product

NovaGuide 2 Intelligent Ultrasound, REFs: NSC-NVGSYS2 & NSC-NVGSYS2-CA

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-2216-2024. 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.