# FDA recall Z-2575-2019

> **Medtronic Vascular** · Class I · device recall initiated 2019-03-15.

## Product

SHERPA NX ACTIVE GUIDING CATHETER, 6F, CHAMP2.0, 55CM.070", REF SA6CHAMP20K.   for cardiovascular use

## Reason for recall

There is a potential for extensive loss of primary segment material exposing underlying stainless-steel braid wires on a subset of 6F Sherpa catheters.

## Distribution

Worldwide distribution to US, Austria, Belgium, Bulgaria, Czech Republic, France, Germany, Greece, Hong Kong, Ireland, Italy, Kazakhstan, Luxembourg, Moldova, Netherlands, Poland, Portugal, Russian Federation, Saudi Arabia, Slovakia, South Africa, Spain, Sweden, Taiwan, and United Kingdom

## Key facts

- **Recall number:** Z-2575-2019
- **Recalling firm:** Medtronic Vascular
- **Classification:** Class I
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2019-03-15
- **Report date:** 2019-10-09
- **Termination date:** 2024-04-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Danvers, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2575-2019

## Citation

> AI Analytics. FDA recall Z-2575-2019. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-2575-2019. Source: US FDA. Licensed CC0.

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