GEHC OEC Injection Cable for MedRad Provis V Contrast Injector — Class II medical device recall Z-2262-2012
Terminated recall by GE OEC Medical Systems, Inc, reported 2012-08-29, distributed nationwide. GE initiated a correction to the instructions/use due to the potential for erroneous auto injection of contras
| Recall number | Z-2262-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE OEC Medical Systems, Inc, Salt Lake City, UT, United States |
| Recall initiated | 2008-10-10 |
| Classified | 2012-08-23 |
| Reported by FDA | 2012-08-29 |
| Terminated | 2013-01-10 |
| Distributed | Nationwide (US) |
| Quantity | 149 units |
| Serial numbers | 82-1138, 82-1586, 82-2089, 82-2117, 82-2182, 82-2214, 82-2226, 82-2262, 82-2264, 82-2308, 82-2312, 82-2314, 82-2321, 82-2328, 82-2380, 82-2391, 82-2438, 82-2483, 82-2512, 82-2516, 82-2535, 82-2722, 82-2796, 82-2821, 82-2846 and 71 more |
Product
GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. In certain fluoroscope X-ray modes, the cable provides a signal to the auto-injector to trigger a contrast injection. Part numbers include 00-902260-01 and 00-883654-01.
Reason for recall
GE initiated a correction to the instructions/use due to the potential for erroneous auto injection of contrast dye.
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-2262-2012. 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.