Centrella™ Bed P7900ARecalls & reported problems
Hill-Rom, Inc. · Hospital Bed · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
Quick summary
This Hill-Rom Centrella hospital bed has 79 reports naming its identifier: no deaths, 1 injury, 78 malfunctions. Most describe torn or split material, unintended movement, or exposed power-cord wires; one report mentions a hip fracture after a fall. One open recall started September 2024 for a bed-exit alert that may fail to reach the nurse call system due to software design. Reports rose to 28 this year from 17 last year.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 84
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 84 adverse event reports that list this exact device (DI 00887761999961), received between Apr 15, 2021 and Sep 8, 2026 — classified as 1 injury, 83 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (61 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Sep 18, 2024Open, Classified
The beds have a potential for an interface issue with the Rauland Responder 5 Nurse Call System where the bed exit system will alert at the bed, but may fail to send a remote alert through the nurse call system.
Z-0228-2025 · Root cause: Software design · FDA record ↗
Most reported problems
Device problems
- Material Split, Cut or Torn61
- Unintended Movement11
- No Audible Alarm4
- Activation Problem3
- Defective Alarm2
- Material Frayed2
- Appropriate Device Problem Term/Code Not Available1
- Improper or Incorrect Procedure or Method1
Patient problems
- No Clinical Signs, Symptoms or Conditions82
- Fall1
- Hip Fracture1
Recent adverse event reports
The 25 most recent of 84 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 8, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50659861 ↗MalfunctionSep 4, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50616115 ↗MalfunctionSep 4, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50616022 ↗MalfunctionSep 3, 2026No Audible Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50587124 ↗MalfunctionSep 2, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50568913 ↗MalfunctionAug 27, 2026Material Split, Cut or Torn
Baxter received a report that the CENTRELLA FRAME power cord had damage with exposed copper wire. This occurred during patient use. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50487152 ↗MalfunctionJul 27, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50045657 ↗MalfunctionJul 8, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25757160 ↗MalfunctionJul 8, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25755956 ↗MalfunctionJun 24, 2026Material Split, Cut or Torn
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME POWER CORD HAD COPPER CONDUCTOR/ WIRES EXPOSED. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25604376 ↗MalfunctionJun 17, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT CENTRELLA FRAME HAD AUXILIARY POWER CORD DAMAGED WITH COPPER WIRES EXPOSED. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25541324 ↗MalfunctionJun 2, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT CENTRELLA FRAME HAD THE AUXILIARY POWER CORD DAMAGED WITH COPPER WIRE EXPOSED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25368732 ↗MalfunctionMay 18, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT CENTRELLA FRAME HAD AUXILIARY POWER CORD DAMAGED WITH COPPER WIRE EXPOSED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25211351 ↗MalfunctionMay 12, 2026Material Split, Cut or Torn
A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME HAD POWER CORD COPPER WIRES EXPOSED. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THERE WERE NO OTHER DEVICES REPORTED TO BE INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25146578 ↗MalfunctionMay 6, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT CENTRELLA FRAME HAD POWER CORD DAMAGED WITH COPPER WIRE EXPOSED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25107540 ↗MalfunctionApr 17, 2026Material Split, Cut or Torn
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA MED-SURG HAD PHYSICALLY DAMAGED POWER CORD COPPER WIRE EXPOSED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24916591 ↗MalfunctionApr 17, 2026Material Split, Cut or Torn
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA MED-SURG HAD PHYSICALLY DAMAGED POWER CORD COPPER WIRE EXPOSED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24916589 ↗MalfunctionMar 20, 2026Material Split, Cut or Torn
ON 25-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME (PRODUCT CODE P7900A000010, SERIAL NUMBER (B)(6)), HAD POWER CORD DAMAGED WITH COPPER WIRES EXPOSED. THIS OCCURRED BEFORE USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24651561 ↗MalfunctionMar 19, 2026No Audible Alarm
ON 20-FEB-2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME (PRODUCT CODE P7900A000011, SERIAL NUMBER (B)(6)), HAD BED EXIT ALARM NOT WORKING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24645776 ↗MalfunctionMar 19, 2026Sparking
ON 20-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME (PRODUCT CODE P7900A000005, SERIAL NUMBER (B)(6)), HAD POWER CORD SPARKED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24645701 ↗MalfunctionFeb 17, 2026Defective Alarm
ON 20-JAN-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME (PRODUCT CODE P7900A000009, SERIAL NUMBER (B)(6)), HAD BED EXIT ALARM NOT ALARMING AT THE NURSE'S STATION. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24367232 ↗MalfunctionFeb 16, 2026Material Split, Cut or Torn
ON 22-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME (PRODUCT CODE: P7900A000019, SERIAL NUMBER: (B)(6), HAD POWER CORD DAMAGED WITH COPPER WIRES EXPOSED. THIS OCCURRED DURING PATIENT USE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24351252 ↗MalfunctionFeb 4, 2026Activation Problem
IT WAS REPORTED THAT CENTRELLA FRAME (PRODUCT CODE P7900A000026, SERIAL NUMBER (B)(6) , THE CPR HANDLES NOT WORKING UNABLE TO ACTIVATE CPR FEATURE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24262001 ↗InjuryJan 14, 2026Improper or Incorrect Procedure or Method
IT WAS REPORTED A PATIENT FELL FROM A CENTRELLA BED AND SUSTAINED AN INJURY. THE PATIENT WAS PUT ONTO THE BED. THE MEDICAL STAFF ¿ZEROED THE BED;¿ HOWEVER, THE BED ALERTED THE STAFF THAT THE ¿¿PATIENT WEIGHT TOO LOW-UNABLE TO SET BED ALARM¿. THE PATIENT WEIGHED 68LBS, AND PER THE INSTRUCTIONS FOR USE STATE THE BED ¿IS INTENDED FOR PATIENT POPULATIONS WEIGHING AT LEAST 70LBS (32 KG) AND IS CAPABLE OF SUPPORTING PATIENTS UP TO 500LBS (227 KG).¿ THE BED EXIT ALARM COULD NOT BE SET, AND SUBSEQUENTLY THE PATIENT FELL FROM THE BED AND SUSTAINED A HIP FRACTURE. THE PATIENT REQUIRED UNSPECIFIED TREATMENT AT THE HOSPITAL. ADDITIONALLY, NO BED MALFUNCTION WAS REPORTED. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Hip Fracture
MAUDE report 24071513 ↗MalfunctionJan 12, 2026Material Split, Cut or Torn
ON 16-DEC-2025, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CENTRELLA FRAME (PRODUCT CODE P7900A000010, SERIAL NUMBER (B)(6)), HAD POWER CORD DAMAGED WITH COPPER WIRE EXPOSED. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24048486 ↗
Other BED, AC-POWERED ADJUSTABLE HOSPITAL devices
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- VersaCare® Med Surg Bed P3200KHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL3 deaths1,193 reports
- Medline MDR107002EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death374 reports
- Medline MDR107003EMedline Industries, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall3 deaths362 reports
- InTouch 2141Stryker Corporation · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths361 reports
- Citadel Plus FX811B3B4AMABBArjohuntleigh AB · BED, AC-POWERED ADJUSTABLE HOSPITAL2 deaths358 reports
- TotalCare® Bed P1900QHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL317 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.