Skip to content

Hillrom™ 4058140Recalls & reported problems

Baxter Medical Systems GmbH + Co. KG · Trumpf Medical/Medizin TruLight 1000 / pendant · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761986114), received between May 9, 2022 and May 9, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 9, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

    IT WAS ALLEGED THE TRULIGHT LIGHT HEAD AND SPRING ARM DETACHED AND FELL FROM THE CEILING. NO HARM OR IMPACT TO A SURGICAL PROCEDURE WAS REPORTED. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14337430 ↗

Other Device, medical examination, ac powered devices

All Device, medical examination, ac powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.