# FDA recall Z-1468-2025

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2025-02-25.

## Product

Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, P7520A20S, P7520A21, P7520A22S, P7520A23, P7520A24S, P7520A3, P7520A31, P7520A37, P7520A39, P7520A45, and P7520A4S.

## Reason for recall

The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.

## Distribution

US Nationwide. Global Distribution.

## Key facts

- **Recall number:** Z-1468-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-25
- **Report date:** 2025-04-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1468-2025

## Citation

> AI Analytics. FDA recall Z-1468-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1468-2025. Source: US FDA. Licensed CC0.

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