Hill-Rom® Resident® Long Term Care Bed P870DRecalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00887761000926), received between Sep 30, 2021 and Mar 23, 2026 — classified as 8 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. 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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 23, 2026Unintended Movement

  ON 24-FEB-2026, A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT RESIDENT BED FRAME (PRODUCT CODE P870D000001, SERIAL NUMBER (B)(6), HAD THE BED MOVING ON ITS OWN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24664597 ↗
• MalfunctionFeb 23, 2026Positioning Failure

  ON 26-JAN-2026, A OTHER HEALTH CARE PROFESSIONAL CONTACTED TECHNICAL SERVICE TO REPORT THAT RESIDENT BED (PRODUCT CODE P870CB4851, SERIAL NUMBER (B)(6)), THE HEAD OF THE BED MOVES ON ITS OWN.THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24423359 ↗
• MalfunctionNov 11, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE RESIDENT BED FRAME WEND DOWN WHEN IT WAS POWERED ON. 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 23523412 ↗
• MalfunctionMay 20, 2025Material Frayed; Material Split, Cut or Torn; Material Frayed; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT STATING THAT RESIDENT BED FRAME POWER CORD WAS FRAYED 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 22054079 ↗
• MalfunctionNov 4, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  A CUSTOMER CONTACTED TECHNICAL SERVICE TO REPORT THAT RESIDENT BED FRAME, HAD AN ISSUE, EXPOSED WIRES ON POWER CORD. 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 DEVICE WAS REQUESTED FOR SERVICE/INSPECTION BY BAXTER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20604147 ↗
• MalfunctionOct 25, 2024Device Tipped Over; Device Tipped Over

  IT WAS REPORTED THAT RESIDENT BED FRAME PATIENT RIGHT SIDE SIDERAIL WAS NOT LATCHING IN PLACE. 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 20539115 ↗
• MalfunctionOct 3, 2024Material Split, Cut or Torn; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THAT RESIDENT BED FRAME AC POWER CABLE WAS BROKE WITH EXPOSED COPPER WIRES. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20361748 ↗
• MalfunctionSep 30, 2021Unintended Movement; Unintended Movement

  HILLROM RECEIVED A REPORT FROM THE ACCOUNT 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 12555730 ↗