# FDA recall Z-1482-2023

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2023-03-31.

## Product

Hill-Rom pro+ mattress, product codes (REF):  a) 20877002S, b) 20877003S, c) 20877004S, d) 20877007S, e) 20877008S, f) 21649301S, g) 21649401S, h) 21649402S, i) P006800A01, j) P006800A02, k) P3255A01, l) P3255A02, m) P3255A03, n) P3255ARENT01, o) P7923A01, p) P7923A02, q) P7923A03, r) P7923A04, s) P7924A01, t) P7924A02, u) P7924A03, v) P7924A04, w) P7924ARENT01

## Reason for recall

There is a potential for mattress cover damage (delamination) which may result in fluid absorption in the mattress (fluid ingress).

## Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Qatar.

## Key facts

- **Recall number:** Z-1482-2023
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-03-31
- **Report date:** 2023-05-10

- **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-1482-2023

## Citation

> AI Analytics. FDA recall Z-1482-2023. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1482-2023. Source: US FDA. Licensed CC0.

---

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