ARROW INTERNATIONAL, LLC recalls

12 recalls on record · latest: April 10, 2026

Official U.S. recall history for ARROW INTERNATIONAL, LLC, compiled from official government records.

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ARROW INTERNATIONAL, LLC recalls Cannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, CS-15552-VSP, CSD-15…

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

ARROW INTERNATIONAL, LLC recalls NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-15232-SFX, CS-15272…

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

ARROW INTERNATIONAL, LLC recalls Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

ARROW INTERNATIONAL, LLC recalls Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15…

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

ARROW INTERNATIONAL, LLC recalls Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive was incorrec…

ARROW INTERNATIONAL, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 Thi…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive were incorre…

ARROW INTERNATIONAL, LLC recalls Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive was incorrec…

ARROW INTERNATIONAL, LLC recalls PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)2…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive was incorrec…

ARROW INTERNATIONAL, LLC recalls FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code:…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive was incorrec…

ARROW INTERNATIONAL, LLC recalls ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive was incorrec…

ARROW INTERNATIONAL, LLC recalls ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J03…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive was incorrec…

ARROW INTERNATIONAL, LLC recalls MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206…

March 11, 2026 · Medical device recalls Moderate risk Due to receiving a notice from a supplier that the liquid adhesive was incorrec…