Electric Stretcher P8020HRecalls & reported problems
Hill-Rom de México, S. de R.L. de C.V. · Hospital Stretcher · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00887761000988), received between Dec 9, 2024 and Jul 3, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Split, Cut or Torn3
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 3, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
BAXTER RECEIVED A REPORT STATING THAT ELECTRIC STRETCHER FRAME POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. 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 22397152 ↗MalfunctionJun 26, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
BAXTER RECEIVED A REPORT STATING THAT ELECTRIC STRETCHER FRAME POWER CORD HAD DAMAGE WITH EXPOSED COPPER WIRES. 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 22338662 ↗MalfunctionMar 12, 2025Unintended Movement; Unintended Movement
BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE ELECTRIC STRETCHER FRAME EXPERIENCED A HILO CYLINDERS SELF RUN. 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 21588014 ↗MalfunctionDec 9, 2024Material Split, Cut or Torn; Material Split, Cut or Torn
DURING SERVICING BY BAXTER, TECHNICAL SERVICE IDENTIFIED THAT ELECTRIC STRETCHER FRAME HAD A DAMAGED POWER CORD WITH EXPOSED COPPER WIRES SHOWING. 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 20880766 ↗
Other STRETCHER, WHEELED, POWERED devices
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- Prime Series 1125Stryker Corporation · STRETCHER, WHEELED, POWERED77 reports
- Prime Series 1125Stryker Corporation · STRETCHER, WHEELED, POWERED71 reports
- Sprint 200 1ES211-1L I N E T spol. s r.o. · Stretcher, Wheeled, Powered1 recall0 reports
- Sprint 200 1ES210-1L I N E T spol. s r.o. · Stretcher, Wheeled, Powered1 recall0 reports
- Prime Series 1125Stryker Corporation · Stretcher, wheeled, powered4 reports
- Prime Series 1125Stryker Corporation · Stretcher, wheeled, powered1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.