# FDA recall Z-1735-2020

> **Boston Scientific** · Class II · device recall initiated 2020-03-09.

## Product

Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor  UPN: M006175272080 (edited 1/13/2021)

## Reason for recall

An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a  procedural delay due to the need to exchange the affected device

## Distribution

Nationwide  Foreign:  Europe, Middle East and Africa, the Americas (North America and South America,   Asia Pacific and  Japan

## Key facts

- **Recall number:** Z-1735-2020
- **Recalling firm:** Boston Scientific
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-03-09
- **Report date:** 2020-04-29

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1735-2020

## Citation

> AI Analytics. FDA recall Z-1735-2020. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1735-2020. Source: US FDA. Licensed CC0.

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