InjuryOUB
MIRADRY SYSTEM
Received Jun 1, 2023 · Event occurred Apr 18, 2023
Report 3008082710-2023-70023 · MDR key 17043211
Device
Generic name
Microwave Dermatologic System
Manufacturer
Miradry Inc.Model number
MN-MD4000-MCCatalog number
MN-MD4000-MC
Product problems
- Adverse Event Without Identified Device or Use Problem
- Adverse Event Without Identified Device or Use Problem
Patient
32 YR · Female
- Cellulitis
- Cellulitis
Narrative
Additional Manufacturer Narrative
A REVIEW OF SYSTEM DATA WAS PERFORMED AND FOUND NO ISSUES WITH THE DEVICE THAT CAUSE THE ADVERSE EVENT.
Description of Event or Problem
PT DEVELOPED CELLULITIS POST TX. THE DOCTOR PERFORMED A SONOGRAM. THEY WERE PRESCRIBED KEFLEX AND CLINDAMYCIN - 3 WEEKS POST TX THE INFECTION WAS NO LONGER PRESENT. THE AREA IS NOW OPEN AND DRAINED ON ITS OWN. LEFT UNDERARM STILL SHOWING OPEN WOUND.