ARROW IPN037305Recalls & reported problems

Teleflex Incorporated · Arrowg+ard Blue Advance(TM) PICC pre-loaded with Arrow(R) VPS Precision(TM) Stylet · Class 2 · Implant

All models of ARROW (1494)

Data updated Oct 16, 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 50801902120774), received between Mar 21, 2024 and Apr 10, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (1 report).

8 other recalls cover devices cleared under the same FDA submission (K153487); they may or may not involve this specific model.

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 16, 2026.

Reports received per month

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

Most reported problems

Device problems

Break1
Material Deformation1

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.

MalfunctionApr 10, 2024Break; Break
IT WAS REPORTED "DILATOR WING BROKE OFF THE SHEATH". NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19078074 ↗
MalfunctionMar 21, 2024Material Deformation; Material Deformation
IT WAS REPORTED " DISTAL TIP OF PEEL AWAY SHEATH BEGAN TO BUCKLE AND FRAY WHILE INSERTING INTO PATIENT. NO MEDICAL INTERVENTION REQUIRED. NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18949099 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K153487. One submission often covers many models, so check the product and lot details in each record.

Z-0001-2024 · Aug 10, 2023 · Open, Classified
Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, REF CDC-45552-VPS2; Catheter: Percutaneous Implanted Long-Ter
Z-1810-2019 · Apr 23, 2019 · Terminated
Arrowg+ard Blue Advance PICC pre loaded with Arrow VPS" Precision Stylet Product Code: CDC 45063 VPS2
Z-1808-2019 · Apr 23, 2019 · Terminated
Arrowg+ard Blue Advance" PICC pre loaded with Arrow VPS" Precision Stylet Product Code: CDC 45041 VPS2
Z-1807-2019 · Apr 23, 2019 · Terminated
Arrowg+ard Blue Advance PICC pre loaded with Arrow VPS" Precision Stylet Product Code: CDC 44063 VPS2
Z-1366-2019 · Dec 13, 2018 · Terminated
Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-44052-VPS2 Product Usage: The Arrow Pressure Injectable PICC is indicated for short-term or longterm peripheral a
Z-1365-2019 · Dec 13, 2018 · Terminated
Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-45052-VPS2 Product Usage: The Arrow Pressure Injectable PICC is indicated for short-term or longterm peripheral a
Z-3199-2018 · Jul 17, 2018 · Terminated
4.5 Fr x 40 cm single-lumen PICC Kit, Product Code CDC-44041-VPS2, 5.5 Fr double-lumen PICC Kit, Product Code CDC-44052-VPS2
Z-3200-2018 · Jul 17, 2018 · Terminated
5.5 Fr x 40 cm double-lumen PICC Kit, Product Code CDC-44052-VPS2

Device details

UDI-DI	`50801902120774`
Brand	ARROW
Model	IPN037305
Catalog no.	CDC-45063-VPS2
Company	Teleflex Incorporated
Product code	LJS · Catheter, intravascular, therapeutic, long-term greater than 30 days
Class	Class 2
FDA submission	K153487
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	Dec 16, 2022

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.

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

Groshong NXT ClearVue Catheter 7617405
Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days
2 deaths1,708 reports
Groshong NXT ClearVue Catheter 7655405
Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days
2 deaths1,536 reports
PowerPICC Catheter 3174118
Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days
1 recall402 reports
L-Cath™ S/L PICC S/L 26GA (1.9F) x 30cm
Argon Medical Devices, Inc. · Catheter,Intravascular,Therapeutic,Long-Term Greater Than 30 Days
2 recalls245 reports
PowerPICC SOLO2 Catheter 1194108D
Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days
2 recalls216 reports
Broviac 0600520
Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days
1 recall265 reports
Groshong® Catheter 7717405
Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days
279 reports
PowerPICC® Catheters 1174108D
Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days
1 recall222 reports

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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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