---
title: "Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AX... — FDA record Z-0764-2024 | Is It on Recall"
description: "A potential for a light system to fall in the operating room."
url: https://isitonrecall.com/recall/fda-device-z-0764-2024-maquet-axcel-axcel-or-light-systems-model-numbers-and-catalog-numbers-axl-5001-ard567501961c-axl-500/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AXL 5001 - ARD567501961C, AXL 5001S - ARD5... — FDA record Z-0764-2024

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 Nov 8, 2023. 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**: Maquet Axcel / Axcel + OR Light Systems, Model Numbers and Catalog Numbers AXL 5001 - ARD567501961C, AXL 5001S - ARD567505961C, AXL 5002 - ARD567501962C, AXL 5002S - ARD567505962C, AXL 5501 - ARD567501960A, AXL 5501 - ARD567501960C, AXL 5501S - ARD567505960C, AXL+5001 DF - ARD567502961C, AXL+5001 SF - ARD567502861C, AXL+5301 DF - ARD567502971C, AXL+5501 DF - ARD567502960C, AXL+5501 SF - ARD567502860C, AXL+5531 DF - ARD567502930C, AXL50 RLC - ARDRLC309000C, AXL50 RLC - ARDRLC309006C, AXL5003 - ARD567505968C, AXL5003 US - ARD567505969C
- **Reason**: A potential for a light system to fall in the operating room.
- **Classification**: Class II
- **Recalling firm**: Getinge Usa Sales Inc
- **Quantity**: 236793 units in total
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0764-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0764-2024%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 | All systems affected |

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

## Distribution

US Nationwide. Global Distribution.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jan 24, 2024
- **Recall initiation date**: Nov 8, 2023
- **Center classification date**: Jan 18, 2024

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-0764-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Getinge Usa Sales Inc records](https://isitonrecall.com/brand/getinge-usa-sales-inc/)
