CARDINAL HEALTH SU130-1411 (UDI 10192253022582)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10192253022582), received between Oct 18, 2020 and Oct 18, 2020 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryOct 18, 2020Break; Break; Difficult to Remove

  CUSTOMER REPORTED THAT RN REMOVED SUCTION FROM THE DRAIN FLAT10MM 30 MINUTES PRIOR TO ATTEMPTED REMOVAL FROM PATIENT¿S ABDOMEN AND OFFERED PAIN RELIEF TO THE PATIENT. RN ATTEMPTED TO REMOVE DRAIN WITHOUT SUCCESS. DISCUSSED WITH MEDICAL TEAM WHO SUGGESTED SHE ATTEMPT AGAIN. FURTHER ATTEMPT RESULTED IN THE DRAIN TUBING SNAPPING AT THE LEVEL OF THE PATIENT¿S ABDOMEN. CONSULTANT REVIEW WAS UNABLE TO RETRIEVE TUBING RETAINED IN ABDOMEN. PATIENT HAD TO RETURN TO OT FOR REMOVAL OF REMAINING TUBING.

  Patient problems: Foreign Body In Patient

  MAUDE report 10694984 ↗