FDA DeviceClass IINotable
FDA Recall: Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)2512
Description
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
Hazard
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
Remedy
85
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