Skip to content

Groshong NXT Catheter 7927507Recalls & reported problems

Bard Access Systems, Inc. · DOT GRO NXT, 5F, · Class 2 · Implant

All models of Groshong NXT Catheter (11)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741035418), received between Aug 23, 2018 and Aug 23, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Expiration Date Error” (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

Device problems

  • Expiration Date Error1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionAug 23, 2018Expiration Date Error

    IT WAS REPORTED THAT THE "PICC LINE PLACED IN PATIENT AND POST INSERTION IT WAS DISCOVERED THAT THE PICC TRAY HAD EXPIRED. TRAY WAS THE SECOND TRAY TO BE REMOVED FROM A NEW BOX ON THE PURCHASING SHELF." IT IS UNKNOWN IF THE FIRST TRAY WAS ALSO EXPIRED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7810135 ↗

Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices

All Catheter,intravascular,therapeutic,long-term greater than 30 days devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page