Bard® Silicone Uretero-Intestinal Anastomosis Urinary Diversion Stent 089008Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10801741011655), received between Apr 14, 2022 and Apr 26, 2022 — classified as 4 injuries, 3 malfunctions.

The most frequently reported specific device problem is “Migration” (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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryApr 26, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT CUSTOMER MENTIONED ABOUT STENT MIGRATION AND URINARY TRACT INFECTION WHEN THEY WERE ASKED OF THE COMPLICATIONS WHILE USING THE URINARY DIVERSION STENT. MEDICAL INTERVENTION WAS UNKNOWN.

  Patient problems: Urinary Tract Infection

  MAUDE report 14206775 ↗
• MalfunctionApr 26, 2022Migration; Migration

  IT WAS REPORTED THAT CUSTOMER MENTIONED ABOUT STENT MIGRATION AND URINARY TRACT INFECTION WHEN THEY WERE ASKED ABOUT THE COMPLICATIONS FACED WHILE USING THE URINARY DIVERSION STENT. NO MEDICAL INTERVENTION WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14206137 ↗
• InjuryApr 26, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT SURVEY RESPONDENT MENTIONED ABOUT URINARY TRACT INFECTION WHEN THEY WERE ASKED ABOUT THE COMPLICATIONS FACED WHILE USING THE URINARY DIVERSION STENT. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED FOR THE URINARY TRACT INFECTION.

  Patient problems: Urinary Tract Infection

  MAUDE report 14206135 ↗
• InjuryApr 21, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE SURVEY RESPONDENT MENTIONED ABOUT URINARY TRACT INFECTION AND IRRITATIVE URINARY SYMPTOMS WHEN ASKED OF COMPLICATIONS WHILE USING THE URINARY STENT. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED.

  Patient problems: Unspecified Kidney or Urinary Problem; Urinary Tract Infection

  MAUDE report 14166323 ↗
• MalfunctionApr 20, 2022Migration; Migration

  IT WAS REPORTED THAT THE SURVEY RESPONDENT MENTIONED ABOUT URGENCY, SURGICAL SITE INFECTION, URINARY TRACT INFECTION AND STENT MIGRATION WHEN ASKED ABOUT THE COMPLICATIONS FACED WHILE USING THE URINARY STENT. NO MEDICAL INTERVENTION WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14161778 ↗
• InjuryApr 20, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE SURVEY RESPONDENT MENTIONED ABOUT URGENCY, SURGICAL SITE INFECTION, URINARY TRACT INFECTION AND STENT MIGRATION WHEN ASKED OF COMPLICATIONS WHILE USING THE URINARY STENT. IT WAS UNKNOWN WHAT MEDICAL INTERVENTION WAS PROVIDED.

  Patient problems: Micturition Urgency; Post Operative Wound Infection; Urinary Tract Infection

  MAUDE report 14161176 ↗
• MalfunctionApr 14, 2022Calcified; Calcified

  IT WAS REPORTED THAT THE SURVEY RESPONDENT MENTIONED ABOUT URGENCY, FLANK PAIN, HEMATURIA AND STENT ENCRUSTATION WHEN THEY WERE ASKED OF COMPLICATIONS WHILE USING THE URINARY DIVERSION STENT. MEDICAL INTERVENTION WAS UNKNOWN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14110982 ↗