Groshong NXT Catheter 9857505Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741036163), received between Nov 21, 2016 and Dec 11, 2019 — classified as 2 injuries, 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 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryDec 11, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT HAD AN ADVERSE REACTION WHEN PICC WAS INSERTED. SYMPTOMS PASSED AFTER A FEW MINUTES. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Reaction

  MAUDE report 9453561 ↗
• InjuryDec 11, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT HAD AN ADVERSE REACTION WHEN PICC WAS INSERTED. SYMPTOMS PASSED AFTER A FEW MINUTES. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: Reaction

  MAUDE report 9453559 ↗
• MalfunctionNov 21, 2016Fluid/Blood Leak; Hole In Material

  ON (B)(6) 2017 - ADDITIONAL INFORMATION REPORTED BY FACILITY: NO SECURACATH WAS USED ON THE PATIENT. THE NURSE REPORTED THE LINE HAD BEEN IN PLACE FOR ABOUT A WEEK WITH NO ISSUES, BUT THEN NOTICED THE LEAK WHEN SHE WENT TO ADMINISTER THE CHEMO.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6119244 ↗