Groshong NXT Catheter 9827508DRecalls & reported problems
Bard Access Systems, Inc. · Groshong NXT Catheter with Sherlock Tip Location System (TLS) Stylet 5F Maximal Barrier Tray (Dual-Lumen) (45cm) · Class 2 · Implant
All models of Groshong NXT Catheter (11)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741036149), received between Dec 7, 2017 and Mar 12, 2023 — 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
Device problems
- Break2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 12, 2023Break; Break
IT WAS REPORTED BY THE CUSTOMER "A PATIENT WITH A 5F DL GROSHONG NXT PICC HAS HAD THIS CATHETER FOR A LONG TIME. RECENTLY, THE RED HUB OF THE PICC "FELL OFF" AND THE PATIENT REPORTED THAT SHE "CLEANED IT WITH ALCOHOL AND STUCK IT BACK ON". CALLER IN PHARMACY IS LOOKING FOR A REPAIR KIT FOR THE RED LEG. RESPONSE: VERIFIED THAT 9827508D IS A 5F DL GROSHONG NXT PICC. EXPLAINED THE NXT IS NOT POWER INJECTABLE. INFORMED THE NXT IS MADE OF SILICONE AND HAS A MAX OF 25 PSI. INFORMED THAT THERE IS A RISK OF INFECTION DUE TO THE HUB FALLING OFF AND PATIENT CLEANING AND PUTTING IT BACK ON. INFORMED HIM THAT THE NXT CAN BE REPAIRED SINCE IT IS NOT POWER INJECTABLE. PROVIDED VALID AND AVAILABLE CODES FOR REPAIR."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16527268 ↗MalfunctionDec 7, 2017Break
FACILITY REPORTED TO THE SALES REP THAT THE GROSHONG DUAL LUMEN PICC WAS PLACED ON (B)(6) 2017. THE PATIENT STATED THAT SHE HEARD HER PUMP BEEPING, LEANED FORWARD IN HER CHAIR AND THEN HEARD A SNAP. THE CATHETER BROKE AT THE HUB AND IT WAS STATED THERE WAS NO EVIDENCE OF THE CATHETER BEING STRETCHED AS IT APPEARED TO HAVE BEEN A QUICK ACTION. THE REMAINDER OF THE CATHETER WAS SUCCESSFULLY REMOVED FROM THE PATIENT WITH OUT INJURY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7094646 ↗
Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices
- Groshong NXT ClearVue Catheter 7617405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 deaths1,708 reports
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- PowerPICC SOLO2 Catheter 1194108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls216 reports
- Broviac 0600520Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall265 reports
- Groshong® Catheter 7717405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days279 reports
- PowerPICC Catheter 3275118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days272 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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