MalfunctionBSF
MEDISORB
Received Mar 12, 2020 · Event occurred Mar 10, 2020
Report MW5093730 · MDR key 9829048
Device
Product problems
- Defective Device
Patient
Not reported
- No Known Impact Or Consequence To Patient
- No Known Impact Or Consequence To Patient
Narrative
Description of Event or Problem
PRODUCT DEFECT DISCOVERED DURING ANESTHESIA PRE-CHECK. FDA SAFETY REPORT ID# (B)(4).