# FDA recall Z-1332-2024

> **D.O.R.C. Dutch Opthalmic Research Center Intl B.V.** · Class II · device recall initiated 2024-01-15.

## Product

Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)

## Reason for recall

When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the  laser fiber tip precisely.

## Distribution

US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.

## Key facts

- **Recall number:** Z-1332-2024
- **Recalling firm:** D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-15
- **Report date:** 2024-03-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Zuidland, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1332-2024

## Citation

> AI Analytics. FDA recall Z-1332-2024. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1332-2024. Source: US FDA. Licensed CC0.

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