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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.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-42703-SJH
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Fea
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Fea
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Cathete
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Cathete
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip¿, ARROWg+ard Blue PLUS¿ Catheter, S
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue PLUS¿ Pressure Injectable Multi-Lumen CVC Kit; Product Codes: CDC-45703-P1A; CDC-45703-PB1A; CDC-42703-P
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit; Product Code: ASK-42802-PWHC1
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue PLUS¿ Pressure Injectable Two-Lumen CVC Kit; Product Code: CDC-42802-P1A
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit; Product Codes: CDC-42854-P1A and CDC-45854-P1A
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Codes: ASK-42703-PAM
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Fe
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue(R) Central Venous Catheterization Kit; Product Code: ASK-24306-WHC1 and ASK-24306-WHC2
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter and Sharps Safety Featu
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) Access Device, Integral Hemostasis Valve and Sharps
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7-7.5 Fr. Catheters; Product Code: ASK-21142
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-15703-PVH and ASK-15703-PNYP
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-15703-PHMC
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Sharps Safety Features
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Code: ASK
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port and Sharps Safety Features (Recommended for
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port for use with 7.5 - 8 Fr. Catheters; Product
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Arrow-Flex(R) Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath and Integral Hemostasis Valve/Side Port
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Codes:
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit with Sharps Safety Features; Product Codes: ASK-04120-HF
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Artery Catheterization Kit with Sharps Safety Features; Product Codes: ASK-04020-RIHM
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Arterial Catheterization Kit; Product Codes: ASK-04020-DH
Hazard: Product sterility may be compromised due to unsealed packaging.