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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 Radial Artery Catheterization Kit; Product Codes: ASK-04020-AH, ASK-04020-MIHS, ASK-04120-HF1
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-04018-OH1
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Radial Arterial Access Kit; Product Code: ASK-04001-BID2
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Maximal Barrier Drape; Product Code: ASK-04000-HMC
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Maximal Barrier Drape; Product Code: ASK-01000-UPMS
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Maximal Barrier Drape; Product Codes: ASK-00376-SU
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Maximal Barrier Drape; Product Codes: ASK-00002-1A
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Maximal Barrier Drape; Product Codes: ASK-00001-1A
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls SnapLock" Catheter/Syringe Adapter; Product Code: AS-05500
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Epidural Needle; Product Codes: AN-05501 and AN-05505
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Spring Wire Guide Introducer Needle; Product Codes: AN-04320 and AN-04418
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Echogenic Introducer Needle; Product Code: AN-04318
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Continuous Nerve Block Needle; Product Codes: AB-00090, AB-00150, AB-17040-N, AB-17080-N, AB-17110-N, AB-17140-N, AB-18
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Catheter Hemostasis Valve For use with .038" (.096 cm) dia. and smaller guide wires; Product Code: AI-07000
Hazard: Product sterility may be compromised due to unsealed packaging.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue¿ Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions (1) Part Number (PN): CDC-22122-1A
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls AGB+ Multi Lumen CVC Kit (1) Part Number (PN): CDC-42703-B1A, (2) PN: CDC-42802-1A, (3) CDC-45703-1A, (4) CDC-45703-A1A,
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue(R) PSI Kit, (1) For use with 7 - 7.5 Fr. Catheters Part Number (PN): ASK-29804-UHN2; (2) For use with 7.
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWg+ard Blue¿ CVC Kit (1) Part Number (PN): CDC-24301-1A, (2) PN: CDC-24306-1A; (3) ARROWg+ard Blue¿ Large-Bore Multi
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls (1) Access Tray, Part Number (PN): ASK-04001-MS; Arrow Multi-Lumen CVC Kit (2) PN: CDC-12703-1A; (3) PN: CDC-15703-1A; (
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls (1) Central Venous Catheterization Kit, Part Number (PN): ASK-04300-PHP; (2) Single-Lumen Central Venous Catheterization
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls (1) Arterial Catheterization Kit, Part Number (PN): ASK-04018-CC; (2) Arterial Line Kit with Sharps Safety Features, PN:
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls (1) Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Bar
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls Multi-Lumen Hemodialysis Catheterization Kit for High Volume Infusions, Part Number: CDC-12123-P1A
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard Technology, Part Numbers: (1) ASK-45541-RWJ4; (2) ASK-45552-RWJ4
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls AGB+ Multi Lumen Central Venous Catheterization (CVC) Kit (1) Part Number: AK-42703-P1A; (2) AK-45703-P1A; (3) AK-45703-
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls Arrow¿ Pressure Injectable Two-Lumen PICC Kit, Product Number: EU-05052-HPMSB
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls (1) ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters, Product Number: A
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 18, 2018Medical DevicesFDA
Arrow International Inc recalls (1) MAC Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters, Product Number: ASK-11242-PHP; (2) Arrow
Hazard: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls Pneumothorax Kit
Hazard: Product packaging may not be completely sealed.
April 11, 2018Medical DevicesFDA
Arrow International Inc recalls ArrowClarke" PleuraSeal¿ Thoracentesis Kit
Hazard: Product packaging may not be completely sealed.