FDA DeviceClass IINotable
FDA Recall: ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331
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
675
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