Official recall notice
FDA DeviceClass IINotable
FDA Recall: Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)1080
- 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
5
Product description
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured