# FDA recall Z-2365-2019

> **Bausch & Lomb Inc Irb** · Class II · device recall initiated 2016-07-11.

## Product

Laseredge 1.1mm Arrow Knife Angled, REF E7592    Product Usage:  Available to surgeons for use in ophthalmic surgical procedures.

## Reason for recall

Possible dull knife edge

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2365-2019
- **Recalling firm:** Bausch & Lomb Inc Irb
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2016-07-11
- **Report date:** 2019-09-04
- **Termination date:** 2019-08-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rochester, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2365-2019

## Citation

> AI Analytics. FDA recall Z-2365-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2365-2019. Source: US FDA. Licensed CC0.

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