ARROW INTERNATIONAL, LLC Recalls
8 recalls on record in the United States
ARROW INTERNATIONAL, LLC recalls MAC" Two-Lumen Central Venous Access Kit for use with 7.5 -
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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ARROW INTERNATIONAL, LLC recalls ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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ARROW INTERNATIONAL, LLC recalls ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTAB
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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ARROW INTERNATIONAL, LLC recalls FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERA
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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ARROW INTERNATIONAL, LLC recalls PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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ARROW INTERNATIONAL, LLC recalls Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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ARROW INTERNATIONAL, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI co
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
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ARROW INTERNATIONAL, LLC recalls Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit fo
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
View recall details →