TruLight 4038110Recalls & reported problems
Baxter Medical Systems GmbH + Co. KG · Hillrom™ TruLight 5000 / 3000 Ceiling Single · Class 2
- 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 00887761995925), received between Mar 4, 2024 and Mar 4, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 4, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT WHILE ONE OF THE NURSES WAS MOVING THE HEAD LIGHT, THE TRULIGHT FELL FROM THE SPRING ARM AND HIT THE NURSE ON THE CALF. THE NURSE WAS ADMITTED TO THE ED, RELEASED SHORTLY AFTER, AND RETURNED TO WORK THE DAY AFTER THE REPORTED EVENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT (B)(4) .
Patient problems: Insufficient Information
MAUDE report 18825636 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.