FUSION-DESIGN 80662530Recalls & reported problems
Richard Wolf GmbH · FIBER LIGHT CABLE Ø 2.5MM TL 3M color code green · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04055207026328), received between Oct 1, 2021 and Oct 1, 2021 — classified as 1 injury.
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
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Partial thickness (Second Degree) Burn1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 1, 2021Adverse Event Without Identified Device or Use Problem
THE PURPOSE OF THIS SUBMISSION IS TO CLOSE THIS MDR.
Patient problems: Partial thickness (Second Degree) Burn
MAUDE report 12561276 ↗
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- Olympus WM-DP2Keymed (Medical & Industrial Equipment) Limited · Accessories, Photographic, For Endoscope (Exclude Light Sources)3 reports
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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