Trauma Stretcher P8040HRecalls & reported problems

Summary

The FDA's MAUDE database contains 16 adverse event reports that list this exact device (DI 00887761000995), received between Jun 23, 2021 and Apr 21, 2026 — classified as 16 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (15 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.

Most reported problems

Recent adverse event reports

The 16 most recent of 16 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 21, 2026Unintended Movement

  BAXTER RECEIVED A REPORT THAT TRAUMA 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 24944986 ↗
• MalfunctionFeb 20, 2026Unintended Movement

  ON 27-JAN-2026, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT TRAUMA STRETCHER FRAME (PRODUCT CODE P8040H000492, 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 24402199 ↗
• MalfunctionJan 13, 2026Material Split, Cut or Torn

  ON 24-NOV-2025, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT TRAUMA STRETCHER FRAME (PRODUCT CODE P8040G000126, 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 24057245 ↗
• MalfunctionDec 15, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE TRAUMA STRETCHER FRAME 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 23804731 ↗
• MalfunctionDec 11, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE TRAUMA STRETCHER FRAME HEAD BRAKE CASTERS WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THIS OCCURRED BEFORE USE. 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 23780838 ↗
• MalfunctionDec 1, 2025Unintended Movement; Unintended Movement

  ON 25-NOV-2025, A COMPANY REPRESENTATIVE - SERVICE PERSONNEL CONTACTED TECHNICAL SERVICE TO REPORT THAT TRAUMA STRETCHER FRAME (PRODUCT CODE: P8040H000487, 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 23686684 ↗
• MalfunctionAug 22, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT TRAUMA STRETCHER FRAME BRAKE CASTERS WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22876140 ↗
• MalfunctionApr 29, 2025Unintended Movement; Unintended Movement

  IT WAS REPORTED THAT TRAUMA STRETCHER FRAME (PRODUCT CODE P8040F000091, 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 21927240 ↗
• MalfunctionApr 21, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE TRAUMA STRETCHER FRAME 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 21875813 ↗
• MalfunctionFeb 21, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT TRAUMA STRETCHER FRAME BRAKE CASTERS WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT AND 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 21433258 ↗
• MalfunctionOct 10, 2024Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE BRAKES WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20421701 ↗
• MalfunctionDec 12, 2023Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN STATING THE BRAKE CASTERS WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18312289 ↗
• MalfunctionSep 28, 2023Unintended Movement; Unintended Movement

  HILLROM RECEIVED A REPORT FROM A HILLROM TECHNICIAN STATING THE BED BRAKES WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17836204 ↗
• MalfunctionNov 25, 2022Unintended Movement; Unintended Movement

  HILLROM RECEIVED A REPORT FROM A HILLROM TECHNICIAN STATING THE BED BRAKES WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15865027 ↗
• MalfunctionJul 18, 2022Unintended Movement; Unintended Movement

  HILLROM RECEIVED A REPORT FROM A HILLROM TECHNICIAN STATING THE BED BRAKE WAS NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT / USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15047915 ↗
• MalfunctionJun 23, 2021Unintended Movement; Unintended Movement

  HILLROM RECEIVED A REPORT FROM A HILLROM TECHNICIAN STATING THE BED BRAKES WERE NOT HOLDING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #: (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12050450 ↗