Model NuCARTGN — Class II medical device recall Z-0644-2016
Terminated recall by CompView Medical, LLC, reported 2016-01-20, distributed nationwide. The attachment of the NuCART Spring Arm to the NuCART horizontal boom may come apart if the securing ring (sna
| Recall number | Z-0644-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CompView Medical, LLC, Vancouver, WA, United States |
| Recall initiated | 2015-12-04 |
| Classified | 2016-01-13 |
| Reported by FDA | 2016-01-20 |
| Terminated | 2016-03-31 |
| Distributed | Nationwide (US) |
| Quantity | 10 units |
| Reason classes | device malfunction |
| Lot numbers | 15806CARTXXGAAT, 15924CARTXXAZPH, 15924CARTXXTNNA, 15A01CARTXXCOEN, 15A19CARTXXOHCA, 15A26CARTXXCAK1, 15A26CARTXXCAK2, 15A26CARTXXCAK3, 15A26CARTXXCAK41, 15A26CARTXXCASJ, DX00357, DX00358, DX00359, DX00360, DX00361, DX00362, DX00363, DX00364, DX00365, DX00366, T9993-02-01, T9993-02-02, U0328-02-01, U0328-02-02, U0718-02-01, U0718-02-02, U1033-02-01, U1033-02-02, U1126-02-01, U1126-02-02 |
Product
Model NuCARTGN. The NuCART is a mobile display and image management platform used in Minimally Invasive Surgery (MIS) environments to facilitate the routing and ergonomic display of video signals from source devices to flat-panel monitors. It is tailored for use with an OEC C-arm and Endo-Cam in MIS surgery suites, Ambulatory Surgery Centers, Urology, GI and other suites.
Reason for recall
The attachment of the NuCART Spring Arm to the NuCART horizontal boom may come apart if the securing ring (snap ring) was not installed correctly causing the spring arm to release and detach.
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-0644-2016. 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.