# FDA recall Z-0282-2023

> **Visionsense, Ltd.** · Class II · device recall initiated 2022-10-17.

## Product

VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner)    Product Number: 161-0001

## Reason for recall

Broken Optical fiber cable damage can occur through handling or bending and can lead to loss of functionality and heating/melting of the outer cable surface.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0282-2023
- **Recalling firm:** Visionsense, Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-10-17
- **Report date:** 2022-11-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Petakh Tikva, N/A, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0282-2023

## Citation

> AI Analytics. FDA recall Z-0282-2023. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0282-2023. Source: US FDA. Licensed CC0.

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