MEDLINE
Received Jul 2, 2026 · Event occurred Jun 9, 2026
Report 1417592-2026-03912 · MDR key 25696507
Device
Product problems
- Lack of Effect
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
IT WAS REPORTED BY THE CUSTOMER THAT STATES THE PRODUCT IS NOT ADEQUATELY ABSORBING URINE OR FECES, LEADING TO INCREASED MOISTURE EXPOSURE.
Additional Manufacturer Narrative
IT WAS REPORTED BY THE CUSTOMER THAT STATES THE PRODUCT IS NOT ADEQUATELY ABSORBING URINE OR FECES, LEADING TO INCREASED MOISTURE EXPOSURE. THERE ARE 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.