CompellaSurfaceRecalls & reported problems across all models

We found 3 models of CompellaSurface by Hill-Rom, Inc. in the FDA's device registry (GUDID). Together they are named in 87 adverse event reports in the FDA's MAUDE database, received between Mar 23, 2022 and Sep 24, 2026 — classified as 4 injuries, 83 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (78 reports).

1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

CompellaSurface recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. 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 · Recall details · FDA record ↗

Most reported CompellaSurface problems

CompellaSurface models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Compella™Surface P7810A

  BED, FLOTATION THERAPY, POWERED
  1 recall82 reports
• Compella™Surface P642AREN0100000

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  4 reports
• Compella™Surface P642ACAP0100000

  BED, AC-POWERED ADJUSTABLE HOSPITAL
  1 report

Recent CompellaSurface adverse event reports

The 15 most recent reports across all models, 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 ↗

Other Hill-Rom, Inc. products

• Centrella Bed2 models · 2,021 reports · 2 recalls
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• pro+18 models · 36 reports · 13 recalls
• Voalte Nurse Call2 models · 419 reports · 2 recalls
• ALLEN24 models · 73 reports · 5 recalls
• WatchCare4 models · 0 reports · 4 recalls
• NaviCare Nurse Call Systems3 models · 99 reports · 2 recalls
• Progressa Surface13 models · 8 reports · 1 recall