MalfunctionOAR
IVAS
Received Mar 24, 2026 · Event occurred Mar 3, 2026
Report 24673360 · MDR key 24673360
Device
Generic name
Injector, Vertebroplasty (does Not Contain Cement)
Manufacturer
Stryker CorporationModel number
0306530000Catalog number
0306530000
Lot number
25322012
Patient
NA · Male
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
DURING THE POSTERIOR PORTION OF THE LUMBAR FUSION, THE JAMSHIDI\ACCESS CANNULA DEVICE BROKE X 2. THE BLUE HANDLE BROKE AWAY FROM THE SILVER ACCESS CANNULA TWICE.