Official recall notice
FDA DeviceClass IINotable
FDA Recall: FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-0
- 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
190
Product description
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured