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Baxter Healthcare Corporation recalls Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobil

Recalled April 2, 2025 · FDA recall Z-1468-2025 · Baxter Healthcare

Hazard
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. · FDA Class II
Units
2,126 units
Sold at
US Nationwide. Global Distribution.

Description

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.

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.
Manufacturer(s)
Baxter Healthcare Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Baxter Healthcare Corporation recalls Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobil | RecallWatchUSA