FDA recall Z-1468-2025

Baxter Healthcare Corporation · Class II · device

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

Status
Ongoing
Initiation date
2025-02-25
Report date
2025-04-02
Voluntary/Mandated
Voluntary: Firm initiated
Location
Deerfield, IL, United States

Primary source

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