Official recall notice
FDA DeviceClass IINotable
FDA Recall: Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
- Recall date
- 2026-06-17
- Brand
- AVID Medical, Inc.
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Recommended action
What to do
60 kits
Product description
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.