Official recall notice
FDA DeviceClass IINotable
FDA Recall: PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)108019021
- 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
115
Product description
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured