FDA DeviceClass IINotable
FDA Recall: ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-
Description
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Hazard
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Remedy
395
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