DAAVLIN 7 SERIES (REF 808HO0008CT6)Recalls & reported problems
Daavlin Distributing CO., The · 7 Ser CT 311-8 100-120V 50/60Hz · Class 2
- 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 B280808HO0008CT60), received between Aug 5, 2024 and Aug 5, 2024 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
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.
InjuryAug 5, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT DID NOT CONTACT PRESCRIBING DOCTOR FOR DOSING INFORMATION PRIOR TO TREATING WITH NEW EQUIPMENT. PATIENT HAD SEVERE ERYTHEMA WITH BLISTERING AFTER FIRST TREATMENT. PATIENT REQUIRED MEDICAL ATTENTION AND WAS ADMITTED INTO THE HOSPITAL.
Patient problems: Partial thickness (Second Degree) Burn
MAUDE report 19911558 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.