Channel Drain V072234Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741051623), received between Mar 4, 2026 and Mar 19, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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 16, 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.

• MalfunctionMar 19, 2026Fluid/Blood Leak

  IT WAS REPORTED THAT THE PATIENT HAD A FOLEY CATHETER INSERTED PRIOR TO CESAREAN SECTION. URINE DRAINED IN COLLECTION BAG. WHEN THE SURGERY WAS COMPLETED AND THE BLANKET WAS PULLED BACK, THE FOLEY TUBING AND BULB WERE FOUND TO BE LAYING ON THE BED BETWEEN THE PATIENTS LEG, COMPLETELY OUT OF THE URETHRA. WHEN THE NURSE TRIED TO BLOW UP THE BALLOON AGAIN WITH WATER THERE WAS A SMALL HOLE WHERE THE WATER WAS LEAKING. PER FOLLOW-UP INFORMATION RECEIVED VIA EMAIL ON 12MAR2026, BOTH PRODUCTS ARE AVAILABLE. FOLEY CATHETER WAS REPLACED. NO TROUBLESHOOTING WAS DONE AS BOTH HAD LEAKS THAT WERE NOT REPAIRABLE. THE LOT #NGKR2507 AND NGKW1965.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24644398 ↗
• InjuryMar 4, 2026Patient Device Interaction Problem

  IT WAS REPORTED THAT THERE WAS A COMPLAINT OF INCREASED PAIN, LIMITED MOBILITY, AND THE INCREASED NEED FOR OPIOID MEDICATION WITH THE USE OF WOUND DRAIN.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Pain

  MAUDE report 24506148 ↗