Procedural stretcher P8000HRecalls & reported problems
Hill-Rom de México, S. de R.L. de C.V. · Hospital Stretcher · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This procedural hospital stretcher is a wheeled patient bed. The 360 reports mostly describe brake casters that did not hold the stretcher in place, so the frame moved unexpectedly. The reports record 1 injury, 359 malfunctions 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
- 361
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 361 adverse event reports that list this exact device (DI 00887761000957), received between Apr 26, 2021 and Sep 28, 2026 — classified as 1 injury, 360 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (340 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement340
- Collapse9
- Activation Problem3
- Device Fell3
- Material Split, Cut or Torn3
- Adverse Event Without Identified Device or Use Problem1
- Device Dislodged or Dislocated1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions357
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
- Fall1
- Laceration(s)1
Recent adverse event reports
The 25 most recent of 361 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926253 ↗MalfunctionSep 28, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50926125 ↗MalfunctionSep 28, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50925965 ↗MalfunctionSep 28, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50925879 ↗MalfunctionSep 28, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918645 ↗MalfunctionSep 28, 2026Unintended Movement
Baxter received a report stating that PROCEDURAL STRETCHER FRAME brake casters were 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 50918223 ↗MalfunctionSep 21, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50848839 ↗MalfunctionSep 11, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50743344 ↗MalfunctionAug 31, 2026Unintended Movement
Baxter received a report that the PROCEDURAL STRETCHER FRAME casters moves, brakes not holding while in brake position. 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 50524455 ↗MalfunctionMay 18, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL STRETCHER FRAME HAD BOTH HEAD CASTERS MOVING WHILE IN BRAKE. 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 25211511 ↗MalfunctionMay 15, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT TRANSTAR 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 25187583 ↗MalfunctionMay 14, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25176021 ↗MalfunctionMay 13, 2026Unintended Movement
DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT PROCEDURAL STRETCHER FRAME HAS BRAKES NOT HOLDING. 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.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25160532 ↗MalfunctionMay 12, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25153239 ↗MalfunctionMay 11, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25145091 ↗MalfunctionMay 11, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25144981 ↗MalfunctionMay 11, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25144434 ↗MalfunctionMay 11, 2026Mechanical Problem
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT PROCEDURAL STRETCHER FRAME HAD SIDERAIL FALSE LATCHING. 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 25143975 ↗MalfunctionMay 9, 2026Unintended Movement
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT PROCEDURAL STRETCHER FRAME HAD CASTERS NOT HOLDING. 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. THE CUSTOMER REPORTED THAT THE PRODUCT IS NOT AVAILABLE FOR SERVICE/INSPECTION BY BAXTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25132051 ↗MalfunctionMay 9, 2026Unintended Movement
A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT PROCEDURAL STRETCHER FRAME CASTERS WERE NOT HOLDING.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 25132030 ↗MalfunctionMay 8, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25130902 ↗MalfunctionMay 8, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL STRETCHER FRAME HAD BRAKE CASTERS NOT HOLDING WHILE IN BRAKE. 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 25128975 ↗MalfunctionMay 8, 2026Unintended Movement
A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT PROCEDURAL STRETCHER FRAME CASTERS WERE NOT HOLDING. 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 25128860 ↗MalfunctionMay 8, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25126659 ↗MalfunctionMay 7, 2026Unintended Movement
BAXTER RECEIVED A REPORT THAT PROCEDURAL 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 25119439 ↗
Other STRETCHER, WHEELED devices
- Power-PRO 6506Stryker Corporation · STRETCHER, WHEELED5 deaths472 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
- NA 0747Stryker Corporation · STRETCHER, WHEELED1 recall87 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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