ARROW IPN920650Recalls & reported problems

Teleflex Incorporated · ARROW ENDURANCE(TM) Extended Dwell Peripheral Catheter System · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports: 0
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

May 19, 2023Open, Classified
Potential for catheter separation or leakage
Z-1826-2023 · Root cause: Under Investigation by firm · FDA record ↗

Device details

UDI-DI	`10801902196399`
Brand	ARROW
Model	IPN920650
Catalog no.	EDC-00820
Company	Teleflex Incorporated
Product code	FOZ · Catheter, intravascular, therapeutic, short-term less than 30 days
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	May 8, 2024

Device type (GMDN): Peripheral intravenous cannula

A short, thin tube intended to be inserted into a peripheral vein (typically on the hand/arm) to enable short-term (< 30 days) intravenous (IV) access for administration of fluids/medication and blood sampling. Also referred to as a peripheral IV catheter, it is typically assembled with a dedicated introduction needle, and usually includes connectors, injection ports, and wings for fixation. It is not intended to be advanced to the central vasculature. This is a single-use device.

Other Catheter, intravascular, therapeutic, short-term less than 30 days devices

BD Insyte Autoguard 382523
Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days
660 reports
BD Insyte Autoguard 382533
Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days
2 recalls527 reports
BD PosiFlush 306546
Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days
1 death608 reports
BD Insyte Autoguard Shielded IV Catheter 381823
Becton, Dickinson And Company · Catheter, intravascular, therapeutic, short-term less than 30 days
582 reports
BD Insyte Autoguard 381423
Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days
1 recall528 reports
BD Insyte Autoguard 382544
Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days
1 recall437 reports
BD Nexiva, BD Q-Syte 383536
Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days
2 recalls374 reports
BD PosiFlush 306547
Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days
2 recalls1 death331 reports

All Catheter, intravascular, therapeutic, short-term less than 30 days devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.