Centrella™ Surface P7922ARENT02Recalls & reported problems
Hill-Rom, Inc. · Hospital Bed Surface · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761976979), received between Jan 29, 2025 and Jan 29, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unintended Movement” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 29, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE CENTRELLA MAX MATTRESS, WIDE SIDERAIL FALSE LATCHES; WHEN APPLYING WEIGHT TO THE SIDERAIL MAKES IT COME DOWN. THE BED WAS LOCATED AT THE ACCOUNT. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21265773 ↗
Other BED, FLOTATION THERAPY, POWERED devices
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- pro+ P7924A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED4 recalls3 reports
- pro+ P7924ARENT01Hill-Rom, Inc. · Bed, Flotation Therapy, Powered3 recalls1 death15 reports
- pro+ P3255A02Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls8 reports
- pro+ P7924A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls4 reports
- pro+ P3255A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls3 reports
- pro+ P7923A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls2 reports
- pro+ P7923A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.