# FDA recall Z-2435-2019

> **Integra LifeSciences Corp.** · Class II · device recall initiated 2019-08-07.

## Product

Integra Jarit GEMINI CLAMP 9 1/4 inch - used in vascular and cardiothoracic procedures used for clamping and occluding vessels.    Cat. #140-332

## Reason for recall

A small crack at the box lock corner may after multiple cleaning and sterilization cycles produce an increased risk of corrosion, weakening the instrument and resulting in premature need for replacement and/or breakage of the instrument

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2435-2019
- **Recalling firm:** Integra LifeSciences Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-07
- **Report date:** 2019-09-11
- **Termination date:** 2020-06-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Plainsboro, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2435-2019

## Citation

> AI Analytics. FDA recall Z-2435-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2435-2019. Source: US FDA. Licensed CC0.

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