# FDA recall Z-2057-2019

> **CooperSurgical, Inc.** · Class II · device recall initiated 2019-06-18.

## Product

LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120

## Reason for recall

The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.

## Distribution

Nationwide domestic distribution. International distribution to Canada and Costa Rica.

## Key facts

- **Recall number:** Z-2057-2019
- **Recalling firm:** CooperSurgical, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-18
- **Report date:** 2019-07-31
- **Termination date:** 2020-06-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Trumbull, CT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2057-2019

## Citation

> AI Analytics. FDA recall Z-2057-2019. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-2057-2019. Source: US FDA. Licensed CC0.

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