Hill-Rom®1000 Bed P1160BRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00887761000940), received between Apr 19, 2021 and Aug 7, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 7, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50175303 ↗
• MalfunctionMar 18, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT FROM A BAXTER TECHNICIAN TO REPORT THE HR1000 RAN UP UNINTENTIONALLY. THE DEVICE WAS LOCATED AT THE ACCOUNT. THIS OCCURRED DURING BIOMED 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 21638622 ↗
• MalfunctionApr 19, 2021Intermittent Continuity; Unintended Movement; Intermittent Continuity; Unintended Movement

  HILLROM RECEIVED A REPORT FROM THE CUSTOMER STATING THE HEAD OF THE BED WILL RUN DOWN ON IT'S OWN AND CAN NOT BE RAISED BACK UP. 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 11684837 ↗