Vital Vue 8886828401Recalls & reported problems
Covidien LP · Light Source · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 10884521042445), received between Apr 17, 2019 and Apr 17, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Most reported problems
Device problems
- Break1
- Delivered as Unsterile Product1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 17, 2019Break; Delivered as Unsterile Product; Break; Delivered as Unsterile Product
ACCORDING TO THE REPORTER, THE DEVICE MEMBRANE CRACKED, AND THERE IS A POSSIBLE CONTAMINATION.
Patient problems: No Information
MAUDE report 8522570 ↗
Other ILLUMINATOR, FIBEROPTIC, SURGICAL FIELD devices
- Olympus WA03310AOLYMPUS Winter & Ibe GmbH · Illuminator, Fiberoptic, Surgical Field8 reports
- Olympus WA03300AOLYMPUS Winter & Ibe GmbH · Illuminator, Fiberoptic, Surgical Field7 reports
- Vital Vue 8886828206Covidien LP · ILLUMINATOR, FIBEROPTIC, SURGICAL FIELD4 reports
- Vital Vue 8886828006Covidien LP · ILLUMINATOR, FIBEROPTIC, SURGICAL FIELD2 reports
- Vital Vue 8886828106Covidien LP · ILLUMINATOR, FIBEROPTIC, SURGICAL FIELD1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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