308nm Excimer System XECL-308C, XECL-308DRecalls & reported problems
Chongqing Peninsula Medical Technology Co., Ltd. · 308nm Excimer System is an ultratraviolet light system designed to be used in Dermatological practice for the treatment of psoriasis and vitiligo. The lamp is axenon-chloride excimer lamp which utilizes a XeCl gas mixture to generate specific ultraviolet light at wavelength of 308 nm. It displays the treatment parameters. Users can set the device and fluence on the control touch screen and determine the machine's state and function under the help of colour-coded indicator light. · 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 06971777450036), received between Sep 9, 2026 and Sep 9, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Missing Information” (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.
Reports received per month
Most reported problems
Device problems
- Missing Information1
Patient problems
- Burning Sensation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2026Missing Information
Patient problems: Burning Sensation
MAUDE report 50690816 ↗
Other Light, Ultraviolet, Dermatological devices
- National Biological Corporation UVB-631-9National Biological Corporation · Light, Ultraviolet, Dermatological2 reports
- Zerigo Handheld System HD-02Zerigo Health, Inc. · Light, Ultraviolet, Dermatological2 reports
- National Biological Corporation UHU-318National Biological Corporation · Light, Ultraviolet, Dermatological1 report
- DAAVLIN 7 SERIESDaavlin Distributing CO., The · Light, Ultraviolet, Dermatological1 report
- DAAVLIN 7 SERIESDaavlin Distributing CO., The · Light, Ultraviolet, Dermatological1 report
- DAAVLIN Phothera 600-3DDaavlin Distributing CO., The · LIGHT, ULTRAVIOLET, DERMATOLOGICAL1 report
- Panosol 6-3DDaavlin Distributing CO., The · LIGHT, ULTRAVIOLET, DERMATOLOGICAL1 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.
How reports and recalls are matched · Editorial policy · Report an error on this page