CARDINAL HEALTH JP-HUR910Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00192253022219), received between Nov 21, 2022 and Nov 21, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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.

• MalfunctionNov 21, 2022Break; Break

  CUSTOMER REPORTED THAT DRAIN INSERTION WAS PERFORMED FOR POST BREAST SURGERY PATIENT WITH A DIAGNOSIS OF MALIGNANT TUMOR OF THE BREAST PART, UNSPECIFIED. PATIENT WAS DISCHARGED WITH 2 ROUND SILICONE DRAINS IN THE SURGERY SITE FOR DRAINAGE. ON SEPTEMBER 28 THAT THE DRAIN BROKE IN THE DISTAL PORTION NEAR THE END OF THE DRAIN AND THE PUMP. DRAIN PIECE WAS REPLACED. NO INJURY OR FURTHER SURGERY WAS REPORTED. NO FURTHER INFORMATION WAS PROVIDED UPON REQUEST.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15839722 ↗
• MalfunctionNov 21, 2022Break; Break

  CUSTOMER REPORTED THAT DRAIN INSERTION WAS PERFORMED FOR POST BREAST SURGERY PATIENT WITH A DIAGNOSIS OF MALIGNANT TUMOR OF THE BREAST PART, UNSPECIFIED. PATIENT WAS DISCHARGED WITH 2 ROUND SILICONE DRAINS IN THE SURGERY SITE FOR DRAINAGE. ON (B)(6) 2022, THE DRAIN BROKE IN THE DISTAL PORTION NEAR THE END OF THE DRAIN AND THE PUMP. NO INJURY OR FURTHER SURGERY WAS REPORTED. DEVICE WAS REPLACED. NO FURTHER INFORMATION WAS PROVIDED UPON REQUEST.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15838316 ↗