DAAVLIN 7 SERIES (REF 808HO0004CT6ND)Recalls & reported problems
Daavlin Distributing CO., The · 7 Ser CT 311-4 100-120V 50/60Hz · Class 2
Data updated Oct 13, 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 B280808HO0004CT6ND00), received between Mar 20, 2026 and Mar 20, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Off-Label Use” (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
- Off-Label Use1
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.
InjuryMar 20, 2026Off-Label Use
THIS IS IN RESPONSE TO PREVIOUSLY FILED MAUDE REPORT MW5180372. PATIENT PURCHASED DEVICE FROM THRIFT STORE THAT ADVERTISED IT AS A TANNING BED, AND RECOMMENDED A 6 MINUTE TREATMENT TIME. PATIENT FELT UNCOMFORTABLE "SEVERAL MINUTES" INTO TREATMENT, AND EXPERIENCED SIGNIFICANT ERYTHEMA 12 HOURS LATER, LEADING THE PATIENT, IN CONFUSION, TO SEEK MEDICAL TREATMENT.
Patient problems: Partial thickness (Second Degree) Burn
MAUDE report 24652618 ↗
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
- DAAVLIN Phothera 600-3DDaavlin Distributing CO., The · LIGHT, ULTRAVIOLET, DERMATOLOGICAL1 report
- Panosol 6-3DDaavlin Distributing CO., The · LIGHT, ULTRAVIOLET, DERMATOLOGICAL1 report
- 308nm Excimer System XECL-308C, XECL-308DChongqing Peninsula Medical Technology Co., Ltd. · Light, Ultraviolet, Dermatological1 report
- DAAVLIN 7 SERIESDaavlin Distributing CO., The · Light, Ultraviolet, Dermatological1 report
- National Biological Corporation UHU-318National Biological Corporation · 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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