Home / Brands / ARROW INTERNATIONAL
ARROW INTERNATIONAL Recalls
525 recalls on record · June 27, 2012 to June 24, 2026 · Medical Devices
Recalls by year
12
13
14
15
16
17
18
19
20
21
22
23
24
26
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 Extension Line Slide Clamps; Product codes: SA-09847
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Sheath Adapter with Cath-Gard¿ Catheter Contamination Shield for use with 4 - 7 Fr. Catheters; Product codes: SA-09847
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls VPS TipTracker Stylet Accessory; Product codes: RHY-177-TTSAP
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls VPS Rhythm ECG Accessory Pack ; Product codes: RHY-100-ECGO
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls VPS Rhythm ECG Accessory Pack with Johans Adapter; Product codes: RHY-100-ECGJ
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Arrow PICC with Chlorag+ard Technology; Product codes: PR-44041-BAS, PR-44052-BAS, PR-44063-BAS, PR-45041-BAS, PR-45052
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROW PICC Set; Product codes: PR-35563-HPHNL and PR-35563-HPHNM
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROW PICC Set; Product codes: PR-34052-HPHNM, PR-34063-HPHNM, PR-35041-HPHNM, PR-35052-HPHNM, PR-35541-HPHNL, PR-35541-
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Echogenic Needle; Product codes: PN-00215-E and PN-00217-E
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Peel Away Sheath over Dilator; Product Codes: PL-05041 and PL-05052
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls PICC Catheter Trimmer ; Product Code:PC-00001-T
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Arterial Catheterization Kit; Product Code:NA-04550-1A
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWgard Blue PLUS¿ Multi-Lumen CVC Kit with Blue FlexTip¿ Catheter; Product Code: MSO-45703-AHS
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Percutaneous Sheath Introducer Kit with ARROWgard Blue¿ Sheath and Integral Hemostasis Valve/Side Port for use with 7 -
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls 10 cc Luer-Slip Loss of Resistance Syringe; Product Code: LR-05501
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROW JACC with Chlorag+ard Technology; Product Code: JR-42063-HPHNM and JR-42563-HPHNM
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Arrow-Johans" ECG Adapter for Right Atrial Electrocadiography (RAECG); Product Code: EG-04900
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls 0.2 Micron Flat Epidural Filter; Product Code: EF-05500
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls TheraCath(R) Epidural Catheter; Product Code: EC-05000
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Spring-Wire Guide Introducer Catheter Assembly; Product Code: CN-04018
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Clear Fenestrated Drape with Adhesive; Product Code: CD-00001
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls 8Fr. Catheter Clamp with Fastener; Product Code: CC-00008
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls 7Fr. Catheter Clamp with Fastener; Product Code: CC-00007
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls 5Fr. Catheter Clamp with Fastener; Product Code: CC-00005
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls 4Fr. Catheter Clamp with Fastener; Product Code: CC-00004
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls ARROWgard Blue PLUS Triple-Lumen CVC Kit with Blue FlexTip Catheter; Product Code: ASK-45703-VC
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 and Sharps Safety
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), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Featu
Hazard: Product sterility may be compromised due to unsealed packaging.
June 6, 2018Medical DevicesFDA
Arrow International Inc recalls Double-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.