AngioDynamics NanoKnife Disposable Single Electrode Probes — Class II medical device recall Z-0073-2022
Terminated recall by Angiodynamics, Inc., reported 2021-10-13. Programming issue affected RFID function of a single lot and did not allow the NanoKnife probes to be recogniz
| Recall number | Z-0073-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, Inc., Queensbury, NY, United States |
| Recall initiated | 2020-04-24 |
| Classified | 2021-10-07 |
| Reported by FDA | 2021-10-13 |
| Terminated | 2022-09-20 |
| Countries outside the US | AU, DE, DK, FR, TH |
| Quantity | 37 |
| Lot numbers | 5577754 |
| Model numbers | 20400103 |
Product
AngioDynamics NanoKnife Disposable Single Electrode Probes, Irreversible Electroporation (IRE) Device, 15 cm IRE Single Electrode RFID Activation, PG. Catalog No. 20400103
Reason for recall
Programming issue affected RFID function of a single lot and did not allow the NanoKnife probes to be recognized by the NanoKnife generator.
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-0073-2022. 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.