Medical Device Recall: 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
Baxter Healthcare Corporation · February 25, 2025
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.
Product Description
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.
Distribution
US Nationwide. Global Distribution.
States Affected
NATIONWIDE
Quantity Affected
2,126 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1468-2025
Status: ongoing
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