Official recall notice
FDA DeviceClass IINotable
FDA Recall: ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-
- Recall date
- 2026-04-29
- Category
- Medical Device
- 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
395
Product description
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured