Official recall notice
FDA DeviceClass IINotable
FDA Recall: MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For
- Recall date
- 2026-04-15
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.
Recommended action
What to do
3 boxes
Product description
Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.