Official recall notice
FDA DeviceClass IINotable
FDA Recall: Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters 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
95
Product description
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured