---
title: "DeVilbiss, 525 5-liter Oxygen Concentrator Models 525DS, 525DS-Q — FDA record Z-0724-2023 | Is It on Recall"
description: "The firm has received complaints of the device becoming hot. The firm has updated the user manual to include warnings that applied parts in contact with the pat"
url: https://isitonrecall.com/recall/fda-device-z-0724-2023-devilbiss-525-5-liter-oxygen-concentrator-models-525ds-525ds-q/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# DeVilbiss, 525 5-liter Oxygen Concentrator Models 525DS, 525DS-Q — FDA record Z-0724-2023

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 18, 2022. 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**: DeVilbiss, 525 5-liter Oxygen Concentrator Models 525DS, 525DS-Q
- **Reason**: The firm has received complaints of the device becoming hot. The firm has updated the user manual to include warnings that applied parts in contact with the patient may in some situations exceed 41 degrees Celsius (105.8 degrees Fahrenheit), clarification on expected service life, and the need for maintenance to certain components.
- **Classification**: Class II
- **Recalling firm**: DeVilbiss Healthcare LLC
- **Quantity**: 1004315 (US); 414559 (OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0724-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0724-2023%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 | Model 525DS UDI-DI 00885304000846 All Lots Model 525DS-Q UDI-DI 00885304009689 All Lots |

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

## Distribution

US Nationwide. Foreign distribution pending.

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**: Dec 28, 2022
- **Recall initiation date**: Nov 18, 2022
- **Center classification date**: Dec 19, 2022

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-0724-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [DeVilbiss Healthcare LLC records](https://isitonrecall.com/brand/devilbiss-healthcare-llc/)
