Angiodynamics, Inc.: Medical Device Recall in 2021 - (Recall #: Z-0073-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

AngioDynamics NanoKnife Disposable Single Electrode Probes, Irreversible Electroporation (IRE) Device, 15 cm IRE Single Electrode RFID Activation, PG. Catalog No. 20400103

Product Classification:

Class II

Date Initiated: April 24, 2020

Date Posted: October 13, 2021

Recall Number: Z-0073-2022

Event ID: 88679

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.

Status: Terminated

Product Quantity: 37

Code Information:

lot 5577754

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated