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ARROW INTERNATIONAL Recalls
525 recalls on record · June 27, 2012 to June 24, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Large Volume Abdominal Paracentesis Kit
Hazard: Product packaging may not be completely sealed.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Arterial Access Tray, introducer catheter; Model: GU-04020
Hazard: The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04220
Hazard: The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04122
Hazard: The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04120
Hazard: The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04020-C
Hazard: The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04020
Hazard: The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit; Model: AK-04018
Hazard: The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
April 4, 2018Medical DevicesFDA
Arrow International Inc recalls ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B
Hazard: Certain lots of peripheral catheter systems may be missing the safety latch, intended to minimize the risk of sharps injuries.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to permit venous access to the central circula
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen CVC Kit
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and S
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, Sh
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip, ARROWg+ard Blue PLUS Catheter and
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Cathet
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Featu
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter, Sharps Safety Features a
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features and Maximal Barrier
Hazard: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
March 28, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue PLUS catheter, Catalog Number: ASK-45854-NG Product Usage: The ARROWg+ard Blue PLUS¿ catheter permit
Hazard: Certain lots may be missing information at the bottom of the lid including the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard BLUE PLUS Pressure Injectable Quad- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) central venous access f
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue¿ Large-Bore Multi-Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (<
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit Product Usage: The Arrow¿ CVC is indicated to provide shor
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls AGB+ Pressure Injectable Quad- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Pro
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.
March 21, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Cathe
Hazard: Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.