Personal Catheter™ Intermittent Catheter 62610Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741069147), received between Aug 30, 2017 and Aug 30, 2017 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (1 report).

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 30, 2017Break; Detachment Of Device Component

  IT WAS REPORTED THAT THE END OF THE CATHETER WAS BROKEN OFF.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6829480 ↗
• MalfunctionAug 30, 2017Component Missing

  IT WAS REPORTED THAT THE CATHETER WAS MISSING FROM THE PACKAGING.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6829477 ↗