Official recall notice

FDA DeviceClass IINotable

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

Recall date
2026-04-29
FDA class
Class II

Why it was recalled

Hazard

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Recommended action

What to do

675

Product description

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

Verify with the official notice →
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