Groshong NXT ClearVue Catheter 7617400Recalls & reported problems
Bard Access Systems, Inc. · Groshong NXT ClearVue Catheter Intermediate Tray 4F Single-Lumen · Class 2 · Implant
All models of Groshong NXT ClearVue Catheter (8)
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 00801741045097), received between Oct 12, 2021 and Oct 20, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Component Incompatible” (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
- Component Incompatible2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 20, 2021Component Incompatible; Component Incompatible
IT WAS REPORTED CONNECTOR FAILED ON SATURDAY AND CUSTOMER HAD TO USE A CONNECTOR REPLACEMENT. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12666607 ↗MalfunctionOct 12, 2021Component Incompatible; Component Incompatible
IT WAS REPORTED "WE RECENTLY RECEIVED A NEW BATCH OF PICC LINES FROM BARD. THE PREVIOUS LOT NUMBERS WE HAD, HAD A REPLACEMENT CONNECTOR. WE USED THOSE AND HAD TO ORDER A NEW CASE OF PICC KITS. OUR CRNA WAS PREFORMING A PICC LINE TODAY AND THE CONNECTOR FAILED THAT WAS IN THE KITS. THANK GOODNESS WE HAD EXTRA OF THE CONNECTORS THAT BARD SENT OUT TO PLACE ON OUR RECALLED KITS. THE CRNA WAS ABLE TO FINISH THE PICC LINE. I AM LETTING YOU KNOW THAT WITH THESE KITS WE RECENTLY RECEIVED THE CONNECTOR FAILED." ADD INFO RCVD 09/23/2021: PLACEMENT DATE: (B)(6) 2021. PLACEMENT INFO: PICC LINE LEFT UPPER ARM. WAS THERE PATIENT HARM REPORTED?: NO.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12615940 ↗
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
- Groshong NXT ClearVue Catheter 7655405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 deaths1,536 reports
- PowerPICC Catheter 3174118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall402 reports
- L-Cath™ S/L PICC S/L 26GA (1.9F) x 30cmArgon Medical Devices, Inc. · Catheter,Intravascular,Therapeutic,Long-Term Greater Than 30 Days2 recalls245 reports
- 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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