# FDA recall Z-0870-2021

> **Boston Scientific Corporation** · Class II · device recall initiated 2020-12-15.

## Product

ACUITY Universal Cutter, MODEL 7060 - Product Usage: intended to facilitate guide catheter removal after the Boston Scientific coronary venous lead is positioned.

## Reason for recall

Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters distributed in the US that did not undergo the applicable sterile processing procedure.

## Distribution

US Nationwide distribution including in the states of Tulsa, OK.

## Key facts

- **Recall number:** Z-0870-2021
- **Recalling firm:** Boston Scientific Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-12-15
- **Report date:** 2021-01-27
- **Termination date:** 2023-08-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0870-2021

## Citation

> AI Analytics. FDA recall Z-0870-2021. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0870-2021. Source: US FDA. Licensed CC0.

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