# FDA recall Z-1290-2025

> **LUMENIS, LTD.** · Class II · device recall initiated 2025-01-23.

## Product

(1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System;  (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802, Laser System; and  (3) Lumenis Pulse 120H, REF GA-0008700, Laser System.

## Reason for recall

The initial current in certain chargers may lead to overheating and damage to the power resistors on the Alternating Current (AC) controller during the power-on sequence of the laser system, resulting in the laser system to not power on.

## Distribution

Distribution was made to PA.  There was no government/military distribution.    Foreign distribution was made to Mexico and Spain.

## Key facts

- **Recall number:** Z-1290-2025
- **Recalling firm:** LUMENIS, LTD.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-23
- **Report date:** 2025-03-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Yokne'Am Ilit, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1290-2025

## Citation

> AI Analytics. FDA recall Z-1290-2025. Retrieved 2026-08-03 from https://api.ai-analytics.org/recall/Z-1290-2025. Source: US FDA. Licensed CC0.

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