Groshong NXT ClearVue Catheter 7617408Recalls & reported problems
Bard Access Systems, Inc. · DOT GRO NXT CLRVU, 4F, · 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 00801741035258), received between Mar 4, 2016 and Jan 31, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment Of Device Component” (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
- Detachment Of Device Component1
- Insufficient Device Problem Information1
- Leak/Splash1
Patient problems
- No Known Impact Or Consequence To Patient1
- No Patient Involvement1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 31, 2019Insufficient Device Problem Information
IT WAS REPORTED VIA MS&S PATIENT HAS A 4FR GROSHONG NXT PICC THAT BLEW WHERE IT MEETS THE CONNECTOR (PORTION WITH WRITING ON IT). THE NURSE STATED THAT WHEN ADMINISTERING CONTRAST FOR A CT ANGIOGRAM THE CATHETER BLEW. CATHETER WAS CLAMPED, BUT NEED TO KNOW IF IT IS REPAIRABLE. MS&S EXPLAINED THAT THE 4FR GROSHONG NXT CAN BE REPAIRED WITH A REPAIR KIT. MS&S EMAILED GROSHONG NXT CONNECTOR IFU.
Patient problems: No Patient Involvement
MAUDE report 8295269 ↗MalfunctionMar 4, 2016Detachment Of Device Component; Leak/Splash
FACILITY CONTACT REPORTED THAT A PICC IN A PATIENT LEAKED WHEN THEY WERE INJECTING. THE PICC WAS REMOVED AND CONTACT STATED THAT THEY FOUND THAT THE WIRE THAT REMAINS IN THE PICC HAD SEPARATED. A NEW PICC WAS PLACED. NO PATIENT INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 5481647 ↗
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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