MalfunctionCAF
VIOS LC AEROSOL DELIVERY SYSTEM
Received Jul 13, 2026
Report MW5190649 · MDR key 25796255
Device
Generic name
Nebulizer (direct Patient Interface)
Manufacturer
Pari Respiratory Equipment, Inc.Model number
310F83-LCPatient
NA · Male
- Insufficient Information
Narrative
Description of Event or Problem
THE PATIENT REPORTED CURRENT NEBULIZER IS NOT FUNCTIONING WELL AND NEEDS A REPLACEMENT NEBULIZER. PATIENT DID NOT MISS A DOSE. UNKNOWN IF PATIENT EXPERIENCED AN ADVERSE EVENT. UNKNOWN IF DEFECTIVE DEVICE IS ON HAND FOR RETURN. UNKNOWN IF MD IS AWARE. NO FURTHER INFORMATION PROVIDED. INDICATION: CHRONIC OBSTRUCTIVE PULMONARY DISEASE, UNSPECIFIED. PRODUCT START DATE/PRODUCT LOT NUMBER/EXPIRATION DATE: UNKNOWN, (B)(6) HAS NOT DISPENSED MEDICATION YET.