Recall Z-1415-2022— Baxter Healthcare Corporation
Class II · Ongoing
Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2022-06-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.. Reason: The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development..
- Recalling firm
- Baxter Healthcare Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-06-24
- Firm location
- Deerfield, IL, United States
Product description
Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress, REF P7923A01.
Reason for recall
The failure mode on the affected mattresses can cause a reduction in the performance of the Microclimate Management feature used to pull heat and moisture away from the patient resulting in an increased patient risk of pressure ulcer development.
Data sourced from openFDA. This site is unofficial and independent of the FDA.