MalfunctionCAF
MEDLINE
Received May 21, 2026 · Event occurred Mar 19, 2026
Report 1417592-2026-01544 · MDR key 25248753
Device
Generic name
Nebulizer (direct Patient Interface)
Manufacturer
Medline Industries, LpCatalog number
HUDRHS883U
Product problems
- Infusion or Flow Problem
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Additional Manufacturer Narrative
IT WAS REPORTED THAT THE NEBULIZERS ARE NOT MISTING. THERE WERE NO REPORTS OF DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW UP CARE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS IS A REPORTABLE EVENT. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THIS REPORT WILL BE REOPENED AND REEVALUATED.
Description of Event or Problem
IT WAS REPORTED THAT THE NEBULIZERS ARE NOT MISTING.