# FDA recall Z-0151-2020

> **Xodus Medical Inc** · Class II · device recall initiated 2019-09-19.

## Product

Cautery Tip Cleaner  REF: 30500    Product Usage:  electrosurgical accessory

## Reason for recall

The sterile barrier of some devices may have been affected

## Distribution

Worldwide Distribution - US Nationwide in the States of : CA, ID, IL, LA, MD, NY, OH, OK, TX, VA, WI and OUS: Malaysia, Kuwait, Australia, Canada, UAE, Ireland, Korea, Saudi Arabia, Japan, Mexico

## Key facts

- **Recall number:** Z-0151-2020
- **Recalling firm:** Xodus Medical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-09-19
- **Report date:** 2019-10-23
- **Termination date:** 2024-03-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New Kensington, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0151-2020

## Citation

> AI Analytics. FDA recall Z-0151-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0151-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
