Groshong NXT ClearVue Catheter 7617407Recalls & 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: 1
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741035241), received between Aug 31, 2021 and Oct 29, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (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.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Break1
Fluid/Blood Leak1
Misassembled1

Patient problems

Foreign Body In Patient1
No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

MalfunctionOct 29, 2025Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED EXTERNAL LEAK NOTED IN THE PICC LINE TUBING .THE LEAK WAS IDENTIFIED AND THE CATHETER WAS REMOVED PER OUR POLICY. NO NEW CATHETER WAS INSERTED, THE PATIENT WAS NEAR THE END OF THEIR COURSE OF ANTIBIOTICS AND ONLY MISSED ONE DOSE. PATIENT WAS NOT HARMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23418798 ↗
InjuryAug 31, 2021Break; Misassembled; Break; Misassembled
IT WAS REPORTED BY HEALTHCARE PROFESSIONAL "VAT WAS CONSULTED TO ASSESS LEAKING PICC. DRESSING WAS REMOVED AND FLUSH ATTEMPTED, FLUID LEAKING FROM SITE. TAPER OF CATHETER NOTED TO BE HUBBED INTO THE SKIN. IN ATTEMPT TO SAVE THE LINE, I ATTEMPTED TO RETRACT THE PICC TO ALLOW FOR REPAIR, WHEN THE TAPER WAS REMOVED IT WAS NOTED THE BLUE CATHETER WAS NOT LONGER CONNECTED AND WAS NOT VISIBLE. I WAS UNABLE TO REMOVE THE CATHETER, SITE WAS CLEANED AND A GUARDIVA WAS APPLIED AND COVERED WITH A TEGADERM. SPOKE WITH APN AND RECOMMENDED STAT PORTABLE X RAY TO LOCATE A POTENTIAL INTRAVASCULAR FOREIGN BODY. ALSO CONTACTED IR TO MAKE HER AWARE OF THE SITUATION AND SHE WAS GOING TO TALK WITH ONE OF THE IR ATTENDINGS. PT ENDED UP NEED TO GO TO IR FOR A INTRAVASCULAR FOREIGN BODY REMOVAL." 08/12/2021: WHAT TYPE OF CATHETER SECUREMENT WAS UTILIZED? BD STAT-LOCK PICC PLUS #VPPBFP PLACEMENT DATE: (B)(6) 21 @1005.
Patient problems: Foreign Body In Patient
MAUDE report 12392511 ↗

Device details

UDI-DI	`00801741035241`
Brand	Groshong NXT ClearVue Catheter
Model	7617407
Company	Bard Access Systems, Inc.
Product code	LJS · Catheter,intravascular,therapeutic,long-term greater than 30 days
Class	Class 2
FDA submission	None listed
Implant	Yes
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Feb 2, 2026

Device type (GMDN): Peripherally-inserted central venous catheter

A thin, flexible tube intended to be introduced into a peripheral vein and advanced to a central vein for short- to long-term intravascular access to administer medications (antibiotics), chemotherapeutic agents, nutrients, parenteral solutions, pain management fluids, and sometimes for blood sampling, monitoring of blood pressure and temperature, and for power injection of contrast media; it is not primarily intended for extracorporeal blood therapies such as haemodialysis. Also known as a peripherally inserted central catheter (PICC), it typically includes dedicated accessories to facilitate catheter introduction/function (e.g., Luer hubs, stylet). This is a single-use device.

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

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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