ARROW INTERNATIONAL Recalls

8 recalls found for ARROW INTERNATIONAL. Check if any of your products are affected.

HIGH

FDA DEVICE

FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arrow Epidural...

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

HIGH

FDA DEVICE

Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531(11)251205(10)33F25M0011 The Arrowg+ard technology is intended to provide...

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

HIGH

FDA DEVICE

Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 The MAC Multi-Lumen...

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

HIGH

FDA DEVICE

MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous...

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

HIGH

FDA DEVICE

PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 The Arrow¿ percutaneous sheath introducer permits venous...

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

HIGH

FDA DEVICE

ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 REF ASK-04020-EUH2 UDI code:...

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

HIGH

FDA DEVICE

ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code: (01)10801902133110(17)261231(11)251211(10)33F25L0140 REF ASK-45703-MGH UDI...

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

HIGH

FDA DEVICE

Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is intended for injection or aspiration of fluids. The needle...

Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured

Mar 11, 2026

ARROW INTERNATIONAL

Due to

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ARROW INTERNATIONAL Recalls

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