Hillrom™ 1850955Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887761991354), received between Jul 21, 2021 and Jul 26, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Fell” (1 report).

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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 26, 2022No Apparent Adverse Event; Insufficient Device Problem Information; No Apparent Adverse Event; Insufficient Device Problem Information

  ROBOT-ASSISTED RADICAL PROSTATECTOMY, POSITIONING OF THE PATIENT IN SUPINE, HEAD-DOWN POSITION, SHOULDER SUPPORTS ATTACHED TO THE HEAD SECTION OF THE TABLE, AT THE END OF THE SURGERY AFTER 3.5 H THERE WAS A LOUD CRASH FOLLOWED BY A THUMP SOUND (PATIENT'S HEAD HIT THE FLOOR) HEAD SECTION SUDDENLY BROKE OFF WITHOUT WARNING. NO HARM WAS REPORTED WITH THE EVENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15105406 ↗
• MalfunctionJul 21, 2021Unintended Movement; Device Fell; Unintended Movement; Device Fell

  THE CUSTOMER REPORTED THAT DURING A SURGICAL PROCEDURE THE HEAD OF THE PATIENT DROPPED UNEXPECTED DUE TO A DEFECT HEAD SECTION OF THE OPERATING TABLE. NO INJURY WAS REPORTED IN RELATION TO THIS EVENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12201894 ↗