# FDA recall Z-0073-2022

> **Angiodynamics, Inc.** · Class II · device recall initiated 2020-04-24.

## 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.

## Distribution

Internationally distribution to the countries of Australia, Germany, Denmark, France, and Thailand.

## Key facts

- **Recall number:** Z-0073-2022
- **Recalling firm:** Angiodynamics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-24
- **Report date:** 2021-10-13
- **Termination date:** 2022-09-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Queensbury, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0073-2022

## Citation

> AI Analytics. FDA recall Z-0073-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0073-2022. Source: US FDA. Licensed CC0.

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