Abbott NT2000iX Radiofrequency — Class II medical device recall Z-0209-2024
Ongoing recall by Abbott, reported 2023-11-08. Certain NT2000iX RF generators were serviced using a tool that was subsequently found to be out of tolerance a
| Recall number | Z-0209-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Abbott, Plymouth, MN, United States |
| Recall initiated | 2023-09-28 |
| Classified | 2023-11-02 |
| Reported by FDA | 2023-11-08 |
| Countries outside the US | CO, TW |
| Quantity | 34 devices |
| UPC / GTIN / UDI-DI | 05415067022417 |
| Serial numbers | 16930509, 16983330, 17583407, 17634837, 17783928, 17783930, 17905961, 17928413, 17942357, 17954521, 17991999, 18003310, 18047384, 18102335, 18132017, 18132092, 18493711, 18522937, 18657521, 18666647, 18675068, 18690920, 18709734, 18742997, 19182119 and 9 more |
| Model numbers | RFG-NT-2000 |
Product
Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator
Reason for recall
Certain NT2000iX RF generators were serviced using a tool that was subsequently found to be out of tolerance and therefore may not have provided accurate results for potential capacitance failure.
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-0209-2024. 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.