FDA DeviceClass IINotable
FDA Recall: Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)1080
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
5
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