Innovian CC MS20026Recalls & reported problems
Draeger Medical Systems, Inc. · 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 04049098049801), received between Jan 5, 2024 and Jan 5, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Patient Data Problem” (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
- No Apparent Adverse Event1
- Patient Data Problem1
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.
MalfunctionJan 5, 2024No Apparent Adverse Event; Patient Data Problem; No Apparent Adverse Event; Patient Data Problem
IT WAS REPORTED THAT A NURSE WAS ATTEMPTING TO DOCUMENT AN ADMINISTERED MEDICATION DOSE TO A SPECIFIC PATIENT RECORD BUT NOTICED AFTER ENTERING THE INFORMATION INTO THE INNOVIAN SYSTEM THAT THE INFORMATION WAS RECORDED FOR A DIFFERENT PATIENT INSTEAD. IT WAS VERIFIED THAT ONLY THE RECORDING OF INFORMATION WENT WRONG; THE PATIENTS HAVE RECEIVED CORRECT MEDICATIONS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18452151 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.