Angiodynamics, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1381-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog Number: 20400111 UPN: H787204001110

Product Classification:

Class II

Date Initiated: March 2, 2023

Date Posted: April 19, 2023

Recall Number: Z-1381-2023

Event ID: 91909

Reason for Recall:

Not programmed in accordance with specification. The programming affects the RFID function and does not allow the NanoKnife probes to be recognized by the NanoKnife generator resulting in a delay in procedure

Status: Ongoing

Product Quantity: 10 boxes( 5 probes/box)

Code Information:

UDI-DI: 15051684029643 Lot Number: 5762110

Distribution Pattern:

US Nationwide Distribution: CA,CO, FL, IA, NY, OH

Voluntary or Mandated:

Voluntary: Firm initiated