CareAssist® Bed P1170GRecalls & reported problems
Hill-Rom de México, S. de R.L. de C.V. · Hospital Bed · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Hill-Rom CareAssist hospital bed is an adjustable electric bed used in care settings. Most of the 82 reports describe the bed moving unexpectedly, with brakes not holding and some alarms not sounding. The reports include 1 injury and no deaths. No recalls name this device.
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
- 88
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 88 adverse event reports that list this exact device (DI 00887761000278), received between Jun 1, 2021 and Sep 23, 2026 — classified as 1 injury, 87 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (56 reports).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement56
- No Audible Alarm11
- Material Split, Cut or Torn9
- Activation Problem6
- Collapse2
- Defective Alarm2
- Detachment of Device or Device Component1
- Failure to Sense1
Patient problems
- No Clinical Signs, Symptoms or Conditions86
- Fall2
- Hip Fracture1
Recent adverse event reports
The 25 most recent of 88 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50875536 ↗MalfunctionSep 23, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50875529 ↗MalfunctionSep 21, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50848723 ↗MalfunctionSep 17, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50797055 ↗MalfunctionSep 15, 2026Material Split, Cut or Torn
Baxter received a report stating that CAREASSIST power cord had damage with exposed copper wires. The process step at which the issue occurred was not specified. There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50773970 ↗MalfunctionSep 7, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50652477 ↗MalfunctionAug 31, 2026Unintended Movement
Baxter received a report that CARE ASSIST CA300 had brakes not holding. 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 50533214 ↗MalfunctionAug 13, 2026Defective Alarm
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50243173 ↗MalfunctionAug 13, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50242401 ↗MalfunctionJun 19, 2026Unintended Movement
BAXTER RECEIVED A REPORT STATING THAT CAREASSIST BED BRAKE CASTERS WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT AND OCCURRED DURING BAXTER SERVICING/TESTING. THERE WAS NO PATIENT INVOLVEMENT. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25563966 ↗MalfunctionJun 18, 2026Activation Problem
BAXTER RECEIVED A REPORT THAT CAREASSIST ES155/255/455 HAD CPR FUNCTION NOT ACTIVATING. N ISSUE.. THIS OCCURRED AFTER 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 25555915 ↗MalfunctionJun 11, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT CARE ASSIST CA305 HAD BRAKES NOT HOLDING WHILE IN BRAKE POSITION. 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 25474375 ↗MalfunctionApr 28, 2026Unintended Movement
A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES120 HEAD SECTION WAS SELF RUNNING IN THE UP POSITION. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25011550 ↗MalfunctionApr 18, 2026No Audible Alarm
A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST BED EXIT WAS NOT ALARMING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24919317 ↗MalfunctionApr 13, 2026Material Split, Cut or Torn
BAXTER RECEIVED A REPORT THAT CAREASSIST ES155/255/455 HAD POWER CORD DAMAGED WITH COPPER WIRES SHOWING. 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 24866523 ↗MalfunctionApr 7, 2026Unintended Movement
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES155/255/455 HAD AN ISSUE, BRAKES WERE 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 24807954 ↗MalfunctionMar 13, 2026Unintended Movement
ON 13-FEB-2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT CARE ASSIST CA100 (PRODUCT CODE P1170B0000020, SERIAL NUMBER (B)(6)), HAD BRAKES NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24598069 ↗MalfunctionMar 9, 2026Unintended Movement
ON (B)(6) 2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES100/200/400 (PRODUCT CODE P1170D0000001, SERIAL NUMBER (B)(6)), HAD BRAKES NOT HOLDING. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24553504 ↗MalfunctionMar 9, 2026Material Split, Cut or Torn
ON 10-DEC-2025, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES130/230/430 (PRODUCT CODE P1170E0000052, 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 24552524 ↗MalfunctionMar 9, 2026Unintended Movement
ON 11-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES110/210/410, NUL (PRODUCT CODE P1170D0000006, SERIAL NUMBER (B)(6)), HAD HI-LOW COLUMN RAISED ON ITS OWN. THIS OCCURRED AFTER 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 24550778 ↗MalfunctionMar 9, 2026Unintended Movement
ON (B)(6) 2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES100/200/400 (PRODUCT CODE P1170D0000042, SERIAL NUMBER (B)(6)), HAD BRAKES NOT HOLDING. THIS OCCURRED AFTER 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 24547795 ↗MalfunctionMar 6, 2026Unintended Movement
ON 10-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES (PRODUCT CODE P1170G0000313, SERIAL NUMBER (B)(6)), HAD HEAD MOVING UP BY ITSELF. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24532177 ↗MalfunctionMar 4, 2026Unintended Movement
(B)(6) HOSPITAL NOTIFIED THE DISTRIBUTOR WHICH WAS FURTHER REPORTED TO BAXTER AND REPORTED THAT FOR 1 UNIT OF CARE ASSIST (PRODUCT CODE: P1170B0000029; LOT/ SERIAL NUMBER: (B)(6)) HAD BRAKES NOT HOLDING. THERE WERE PATIENT INVOLVEMENT AND NO INJURY OR ANY IMPACT ON THE PATIENT OR USER RESULTING FROM THIS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24507857 ↗MalfunctionFeb 26, 2026Unintended Movement
ON (B)(6) 2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT CAREASSIST ES (PRODUCT CODE P1170G0000313, SERIAL NUMBER(B)(6)), HAD BRAKES NOT HOLDING. 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 24462026 ↗MalfunctionFeb 23, 2026Activation Problem
ON (B)(6) 2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT CARE ASSIST ES155/255/455 (PRODUCT CODE P1170G0000069, SERIAL NUMBER (B)(6), HAD CPR FEATURE UNABLE TO BE ACTIVATED. THIS OCCURRED AFTER 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 24421713 ↗
Other BED, AC-POWERED ADJUSTABLE HOSPITAL devices
- Centrella™ Bed P7900BHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL2 recalls5 deaths1,937 reports
- Progressa® Bed System P7500AHill-Rom, Inc. · BED, AC-POWERED ADJUSTABLE HOSPITAL1 recall1 death1,377 reports
- 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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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