Official recall notice
FDA DeviceClass IINotable
FDA Recall: COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code: 60884522007028
- Recall date
- 2026-06-10
- Brand
- Covidien LLC
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Due to customer complaint regarding incorrect display box labeling.
Recommended action
What to do
1,002
Product description
Due to customer complaint regarding incorrect display box labeling.