Compella™Surface P7810ARecalls & reported problems
Hill-Rom, Inc. · Hospital Bed Surface Controller · Class 2
Quick summary
This is a Hill-Rom Compella hospital bed surface controller. Most of the 84 reports describe material that split, was cut or tore, and a few mention sparking. There is 1 injury, a report of a pressure injury that worsened while the bed was in use, and no deaths. The 1 recall is closed; it started in February 2022 over damaged power cords that could expose wires and create a risk of shock.
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
- 82
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 82 adverse event reports that list this exact device (DI 00887761013803), received between Jun 5, 2024 and Sep 24, 2026 — classified as 82 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (78 reports).
1 FDA recall record name this device's identifier.
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
- Feb 14, 2022Terminated
Potential damage to the power cord may cause the power conductors to be exposed, thereby creating a risk of shock from the power mains.
Z-0821-2022 · Root cause: Labeling design · FDA record ↗
Most reported problems
Device problems
- Material Split, Cut or Torn78
- Sparking5
- Material Frayed1
- Unintended Electrical Shock1
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions81
- Electric Shock1
Recent adverse event reports
The 25 most recent of 82 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50888490 ↗MalfunctionSep 17, 2026Sparking
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50811282 ↗MalfunctionSep 17, 2026Material Split, Cut or Torn
Baxter received a report that the CNTROLR, RNT power cord had damage with exposed copper wires. This occurred during Baxter servicing/testing. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50805769 ↗MalfunctionSep 17, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50805562 ↗MalfunctionSep 16, 2026Material Split, Cut or Torn
Baxter received a report that CNTROLR, RNT CLRT 120V US had power cord damaged with cooper wires exposed. 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 50782558 ↗MalfunctionSep 8, 2026Sparking; Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50674769 ↗MalfunctionMay 28, 2026Material Split, Cut or Torn
A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CNTROLR, RNT CLRT HAD BLOWER POWER CORD DAMAGED. COOPER EXPOSED. THE PROCESS STEP DURING WHICH THIS OCCURRED WAS UNKNOWN. 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 25313062 ↗MalfunctionMay 20, 2026Material Split, Cut or Torn
DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT AIR SUPPLY W/TURN AST & CM/KG HAD EXPOSED COPPER WIRES. 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 25226532 ↗MalfunctionMay 13, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/TURN AST & IN/LB HAD DAMAGED POWER CORD WITH COPPER WIRE EXPOSED. 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 25159953 ↗MalfunctionMay 7, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT CNTROLR, RNT CLRT 120V US 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 25117726 ↗MalfunctionApr 29, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/TURN AST & CM/KG HAD POWER CORD DAMAGED WITH COPPER EXPOSED. THIS OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25037697 ↗MalfunctionApr 27, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/CLRT & CM/KG UNIT 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 25002688 ↗MalfunctionApr 23, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/CLRT & CM/KG UNIT HAD POWER CORD DAMAGED WITH COPPER WIRES EXPOSED. 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 24974641 ↗MalfunctionApr 14, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/CLRT & IN/LB UNIT HAD POWER CORD DAMAGED WITH COPPER WIRES EXPOSED. THIS OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24877771 ↗MalfunctionApr 11, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT COMPELLA 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 24847668 ↗MalfunctionApr 2, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/CLRT & CM/KG UNIT 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 24772543 ↗MalfunctionApr 2, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/CLRT & IN/LB UNIT HAD POWER CORD DAMAGED WITH COPPER WIRES. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24772507 ↗MalfunctionApr 1, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/TURN AST & IN/LB 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 24760379 ↗MalfunctionApr 1, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT AIR SUPPLY W/CLRT & IN/LB UNIT 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 24759392 ↗MalfunctionMar 18, 2026Material Split, Cut or Torn
ON 20-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT AIR SUPPLY W/CLRT & IN/LB UNIT (PRODUCT CODE P7810ACC3A0ENG1, 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 24634330 ↗MalfunctionMar 18, 2026Material Split, Cut or Torn
ON (B)(6) 2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT AIR SUPPLY W/CLRT & IN/LB UNIT (PRODUCT CODE P7810ACC3A0ENG1, 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 24628498 ↗MalfunctionMar 5, 2026Material Split, Cut or Torn
ON 09-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT AIR SUPPLY W/CLRT & CM/KG UNIT (PRODUCT CODE P7810ACC3A0ENG0, 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 24521283 ↗MalfunctionMar 3, 2026Material Split, Cut or Torn
ON 06-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CNTROLR, RNT CLRT 120V US (PRODUCT CODE P7810ARC3A0ENG1, SERIAL NUMBER (B)(6)), HAD POWER CABLE DAMAGED WITH EXPOSED COPPER WIRES. 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 24502991 ↗MalfunctionMar 2, 2026Material Split, Cut or Torn
ON 12-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CNTROLR, RNT CLRT 120V US (PRODUCT CODE P7810ARC3A0ENG1, 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 24484368 ↗MalfunctionJan 29, 2026Material Split, Cut or Torn
ON 09-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CNTROLR, RNT CLRT 120V US (PRODUCT CODE: P7810ARC3A0ENG1, SERIAL NUMBER: (B)(6), HAD POWER CORD DAMAGED WITH EXPOSED COPPER WIRES. 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 24211101 ↗
Other BED, FLOTATION THERAPY, POWERED devices
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- 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.