---
title: "Dr¿ger Perseus A500 Anesthesia Workstation — FDA record Z-1512-2024 | Is It on Recall"
description: "Unexpected shutdown while operating on battery power."
url: https://isitonrecall.com/recall/fda-device-z-1512-2024-dr-ger-perseus-a500-anesthesia-workstation/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Dr¿ger Perseus A500 Anesthesia Workstation — FDA record Z-1512-2024

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 Mar 20, 2024. 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**: Dr¿ger Perseus A500 Anesthesia Workstation
- **Reason**: Unexpected shutdown while operating on battery power.
- **Classification**: Class I
- **Recalling firm**: Draeger Medical, Inc.
- **Quantity**: 16,841 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1512-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1512-2024%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 | Material No. MX06000; UDI-DI: 04048675253600; All Serial No. |

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

## Distribution

Domestic: Nationwide Distribution; Foreign: Angola, Argentina, Australia, Austria, Bahrain, Belarus, Belgium, Bolivia, Botswana, Brazil, Brunei Dar-se- S, Bulgaria, Canada, Chili, China, Columbia, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, French Polynesia, French Guiana, Georgia, Germany, Gibraltar, Greece, Guadeloupe, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kuwait, Lebanon, Liechtenstein, Lithuania, Malaysia, Maldives, Mauritius, Mayotte, Mexico, Morocco, Netherlands, New Zealand, Norway, Oman, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovenia, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Turkmenistan, Uganda, Ukraine, United Kingdom, Uruguay, United Arab Emirates, Vietnam.

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

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## Dates in the source

- **Report date**: Apr 24, 2024
- **Recall initiation date**: Mar 20, 2024
- **Center classification date**: Apr 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-1512-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Draeger Medical, Inc. records](https://isitonrecall.com/brand/draeger-medical-inc/)
