Official recall notice
FDA DeviceClass IINotable
FDA Recall: 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Ne
- Recall date
- 2026-08-19
- Brand
- BD SWITZERLAND SARL
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Products may not have received adequate sterilization processing.
Recommended action
What to do
93,700
Product description
Products may not have received adequate sterilization processing.