Becton Dickinson Infusion Therapy Systems, Inc.

BD Nexiva Closed IV Catheter System, REF 383530, 24GA 0.56IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383647, 20GA 1.25IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383538, 20GA 1.75IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383531, 24GA 0.75IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383540, 18GA 1.75IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383534, 20GA 1.25IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383539, 18GA 1.25IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383532, 22GA 1.00IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383533, 20GA 1.00IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Q-Syte Vial Access Adapter, 0.16 ml, REF 385108, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

BD Nexiva Closed IV Catheter System, REF 383649, 18GA 1.25IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Nexiva HF Closed IV Catheter System, REF 383537, 20GA 1.25IN, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FOZ·October 19, 2009

BD Q-Syte, Luer Access Split-Septum, 0.10 ml, REF 385100, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

BD Q-Syte Extension Set, 15 cm, P.V. 0.21 ml, REF 385102, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

FDA Adverse Event

Injury ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 6, 2019

BD Q-Syte Extension Set, 15cm Std Bore, P.V. 1.14 ml Luer-Lok, REF 385101, Becton Dickinson Infusion Therapy Systems Inc.

FDA Recall

Terminated ·Becton Dickinson Medical Systems·Product code FPA·October 19, 2009

BD Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.

FDA Recall

Terminated ·Becton Dickinson & Company·Product code FPA·February 19, 2015

Becton Dickinson Ireland Limited

Authorized representative

🇮🇪 Ireland·21 Manufacturers

BD Insyte Autoguard BC, Shielded IV Catheter with Blood Control Technology, REF: 382533, 20 GA x 1.00 in (1.1x25 mm) 63 mL/min, Rx Only. BD Insyte Autoguard BC Shielded IV Catheter is intended to be inserted into a patient's peripheral vascular system for short term use to sample blood, monitor blood pressure, or administer fluids.

FDA Recall

Open, Classified ·Becton Dickinson Infusion Therapy Systems, Inc.·Product code FOZ·June 26, 2024

BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660 mL/hr)-0.5mL, REF 383536; BD Q-Style Luer Access Split Septum BD Vialon Material; BD Instaflash Needle Technology; Rx Only, Sterile EO. BD Nexiva closed IV catheter systems are over-the-needle, intravascular catheters. These devices have a radiopaque BD Vialon" catheter, needle, needle shield, septum, stabilization platform, integrated extension tubing, clamp, dual port adapter, vent plug and pre-attached BD Q-Syte Luer Access Split Septum. The needle and catheter are protected by a needle cover. A BD Q-Syte device or an end cap with protective cover is provided in the unit package. The closed system is designed to keep blood contained within the device throughout the insertion process. The septum is designed to wipe visible blood from the needle surface as the needle is withdrawn from the catheter, further reducing the risk of blood exposure. The needle tip is passively protected when the needle is removed, reducing the risk of accidental needlestick injury. These devices have BD Instaflash" Needle Technology, allowing for immediate visualization of blood along the catheter. Continuous blood return is seen in the extension tubing. The vent plug prevents blood leakage from the extension tubing during insertion. Both the stabilization platform and dual port adapter are color coded to indicate catheter gauge size (24GA (0.7 mm)=Yellow, 22GA (0.9 mm)=Blue, 20GA (1.1 mm)=Pink, 18GA (1.3 mm)=Green). BD Nexiva closed IV catheter systems are intended to be inserted into a patient s vascular system for short term use to sample blood, monitor blood pressure, or administer fluids. These catheters may be used for any patient population with consideration given to adequacy of vascular anatomy, procedure being performed, fluids being infused, and duration of therapy. The 22-18GA (0.9-1.3 mm) devices are suitable for use with power injectors set to a maximum pressure of 300 psi (2068 kPa) when access ports not suitable for use with power injectors are removed.

FDA Recall

Open, Classified ·Becton Dickinson Infusion Therapy Systems Inc.·Product code FOZ·September 8, 2021