---
title: "(1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Puls... — FDA record Z-1290-2025 | Is It on Recall"
description: "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"
url: https://isitonrecall.com/recall/fda-device-z-1290-2025-1-lumenis-pulse-120h-30-amp-ref-ga-2009996-laser-system-2-lumenis-pulse-120h-moses-2-0-dom-ref-ga00/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# (1) Lumenis Pulse 120H 30 amp, REF GA 2009996, Laser System; (2) Lumenis Pulse 120H, Moses 2.0 (DOM), REF GA0006802, ... — FDA record Z-1290-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 23, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: 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.
- **Classification**: Class II
- **Recalling firm**: LUMENIS, LTD.
- **Quantity**: 3 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1290-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1290-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Software version 2.4.1.0. (1) REF GA-2009996 - Serial number 1791, UDI-DI 07290109145518; (2) REF GA-0006802 - Serial number 1803, UDI-DI 07290109145525; and (3) REF-GA0008700 - Serial number 1818, UDI-DI 07290109145464. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)

## Dates in the source

- **Report date**: Mar 12, 2025
- **Recall initiation date**: Jan 23, 2025
- **Center classification date**: Mar 5, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1290-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [LUMENIS, LTD. records](https://isitonrecall.com/brand/lumenis-ltd/)