Transport Stretcher P8005HRecalls & reported problems
Hill-Rom de México, S. de R.L. de C.V. · Hospital Stretcher · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Baxter Transport Stretcher P8005H is a wheeled hospital stretcher used to move patients. Most reports describe the brakes not holding, so the stretcher can roll or move on its own; a few mention falls, including one with a bone fracture. There are 65 reports, with 2 deaths and 1 injury. 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
- 63
- Deaths reported
- 1
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 63 adverse event reports that list this exact device (DI 00887761000964), received between Jun 1, 2022 and Sep 29, 2026 — classified as 1 death, 1 injury, 61 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (60 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 Movement60
- Collapse1
- Improper or Incorrect Procedure or Method1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions61
- Bone Fracture(s)1
- Fall1
Recent adverse event reports
The 25 most recent of 63 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926910 ↗MalfunctionMay 7, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT STD STRETCHER FRAME 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 25118941 ↗MalfunctionApr 22, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT STD STRETCHER FRAME 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 24957750 ↗MalfunctionApr 20, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT TRANSTAR STRETCHER 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 24933695 ↗MalfunctionApr 20, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT TRANSTAR STRETCHER 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 24932074 ↗MalfunctionApr 18, 2026Unintended Movement
A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME BRAKES WERE 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 24919353 ↗MalfunctionMar 30, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT STRETCHER FRAME 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 24733586 ↗MalfunctionMar 11, 2026Unintended Movement
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE BRAKES WERE 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 24572231 ↗MalfunctionMar 5, 2026Unintended Movement
ON 09-FEB-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT TRANSTAR STRETCHER (PRODUCT CODE P8005A000017, SERIAL NUMBER (B)(6)), HAD BRAKE IS 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 24523990 ↗MalfunctionFeb 19, 2026Unintended Movement
ON 23-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT TRANSTAR STRETCHER FRAME (PRODUCT CODE P8000D005533, SERIAL NUMBER (B)(6)), 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 24394237 ↗MalfunctionJan 28, 2026Unintended Movement
ON 07-JAN-2026, A NURSE CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE: P8005H001082, SERIAL NUMBER (B)(6)), 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 24201207 ↗MalfunctionJan 20, 2026Unintended Movement
ON 23-DEC-2025, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005F000165, SERIAL NUMBER (B)(6)), HAD THE 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 24120557 ↗MalfunctionJan 19, 2026Unintended Movement
ON 22-DEC-2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005F000032, 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 24109117 ↗MalfunctionJan 15, 2026Unintended Movement
ON (B)(6) 2025, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE: P8005H000988, 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 24083369 ↗MalfunctionJan 14, 2026Unintended Movement
ON 03-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005G000012, SERIAL NUMBER (B)(6), 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 24069775 ↗MalfunctionJan 13, 2026Unintended Movement
ON 28-DEC-2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005H000140, SERIAL NUMBER (B)(6)), HAD TWO BRAKE CASTERS NOT HOLDING. 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 24055701 ↗MalfunctionJan 6, 2026Unintended Movement
ON 09-DEC-2025, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT TRANSTAR STRETCHER (PRODUCT CODE P8005A000002, SERIAL NUMBER (B)(6)), HAD THE BRAKE 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 23974521 ↗MalfunctionJan 5, 2026Unintended Movement
ON (B)(6) 2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005G000012, SERIAL NUMBER (B)(6), HAD BRAKES NOT HOLDING WHEN BRAKES ARE SET. 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 23967206 ↗MalfunctionDec 5, 2025Unintended Movement; Unintended Movement
DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT STD STRETCHER FRAME (PRODUCT CODE: P8005G000030, SERIAL NUMBER: (B)(6), HAD BRAKES NOT HOLDING. 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 23730385 ↗MalfunctionDec 1, 2025Unintended Movement; Unintended Movement
ON 21-NOV-2025, A COMPANY REPRESENTATIVE: SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005H000972, SERIAL NUMBER (B)(6)), 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 23687327 ↗MalfunctionNov 25, 2025Unintended Movement; Unintended Movement
ON (B)(6) 2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005H000714, SERIAL NUMBER (B)(6)), HAD FOOT 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 23648517 ↗MalfunctionNov 21, 2025Unintended Movement; Unintended Movement
ON (B)(6) 2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005H000796, SERIAL NUMBER (B)(6), 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 23623829 ↗MalfunctionNov 21, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE TRANSTAR STRETCHER BRAKE CASTERS WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. 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. THE CUSTOMER DID NOT COMMUNICATE THIS EVENT TO ANOTHER BAXTER DEPARTMENT OR AUTHORITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23619416 ↗MalfunctionNov 21, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE PROCEDURAL STRETCHER FRAME FOOT BRAKE CASTERS WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THIS OCCURRED DURING BAXTER SERVICING/TESTING. 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 23619236 ↗MalfunctionNov 10, 2025Unintended Movement; Unintended Movement
ON (B)(6) 2025, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT STD STRETCHER FRAME (PRODUCT CODE P8005F000109, SERIAL NUMBER (B)(6)), 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 23512806 ↗
Other STRETCHER, WHEELED devices
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- Procedural stretcher P8000HHill-Rom de México, S. de R.L. de C.V. · STRETCHER, WHEELED361 reports
- Prime Series 1115Stryker Corporation · STRETCHER, WHEELED1 death251 reports
- Prime Series 1115Stryker Corporation · STRETCHER, WHEELED1 recall199 reports
- Power-PRO 2, High Configuration 650705550001Stryker Corporation · STRETCHER, WHEELED2 recalls2 deaths99 reports
- NA 1089Stryker Corporation · STRETCHER, WHEELED175 reports
- NA 5050Stryker Corporation · STRETCHER, WHEELED1 recall99 reports
- Power-PRO 2 650700000000Stryker Corporation · STRETCHER, WHEELED2 recalls1 death42 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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