FDA Device recall Z-1381-2023
NanoKnife 5-Probe Procedure Pack 15 cm - Activation
- FDA Device
- Class II
- ongoing
- Published 2023-04-19
On 2023-04-19 the FDA classified a Class II recall of NanoKnife 5-Probe Procedure Pack 15 cm - Activation by Angiodynamics, citing 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 resu….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1381-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-02 |
| Published | 2023-04-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Angiodynamics |
| Distribution | US |
Product
NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog Number: 20400111 UPN: H787204001110
Reason
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
Identifiers
| code_info | UDI-DI: 15051684029643 Lot Number: 5762110 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1381-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.