# FDA recall Z-2227-2025

> **Philips Respironics, Inc.** · Class I · device recall initiated 2025-06-30.

## Product

DreamStation Auto CPAP. Non-Continuous Ventilator.

## Reason for recall

Devices may possess a programming error resulting in an incorrect device configuration.

## Distribution

Worldwide - US Nationwide in the states of AL, CA, CO, FL, GA, IN, LA, MD, NE, NJ, NY, PA, TX & DC. The country of France.

## Key facts

- **Recall number:** Z-2227-2025
- **Recalling firm:** Philips Respironics, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-30
- **Report date:** 2025-08-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Murrysville, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2227-2025

## Citation

> AI Analytics. FDA recall Z-2227-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2227-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*