# FDA recall Z-1381-2023

> **Angiodynamics, Inc.** · Class II · device recall initiated 2023-03-02.

## Product

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

## 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

## Distribution

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

## Key facts

- **Recall number:** Z-1381-2023
- **Recalling firm:** Angiodynamics, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-02
- **Report date:** 2023-04-19

- **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-1381-2023

## Citation

> AI Analytics. FDA recall Z-1381-2023. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1381-2023. Source: US FDA. Licensed CC0.

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