INFUSE BONE GRAFT
Report
- Report Number
- 1030489-2014-03346
- Event Type
- Injury
- Date Received
- July 29, 2014
- Report Date
- April 28, 2015
- Manufacturer
- MEDTRONIC SOFAMOR DANEK USA, INC
- Product Code
- NEK
- PMA / PMN Number
- P000058
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- LA, US
- Reporter Occupation
- ATTORNEY
Narratives
(B)(4). NEITHER THE DEVICE NOR FILMS OF APPLICABLE IMAGING STUDIES WERE RETURNED TO THE MANUFACTURER FOR EVALUATION. THEREFORE, WE ARE UNABLE TO DETERMINE THE DEFINITIVE CAUSE OF THE REPORTED EVENT. PRODUCTS FROM MULTIPLE MANUFACTURERS WERE IMPLANTED DURING THE PROCEDURE. ALTHOUGH IT IS UNKNOWN IF ANY OF THE DEVICES CONTRIBUTED TO THE REPORTED EVENT, WE ARE FILING THIS MDR FOR NOTIFICATION PURPOSES.
UPDATED INFORMATION: "IT WAS REPORTED THAT ON (B)(6) 2009: THE PATIENT UNDERWENT FUSION SURGERY. FOLLOWING IMPLANTS WERE USED: INFUSE BONE GRAFT. MASTERGRAFT. FLOSEAL HEMOSTATIC MATRIX (BAXTER HEALTH FOUNDATION). CRUSHED CANCELLOUS X4 (MUSCULOSKELETAL TRANSPLANT FOUNDATION)".
IT WAS REPORTED THAT THE PATIENT DEVELOPED UNSPECIFIED INJURIES FOLLOWING THE USE OF RHBMP-2/ACS IN AN UNSPECIFIED SPINAL FUSION SURGERY. NO ADDITIONAL INFORMATION WAS REPORTED.
"IT WAS REPORTED THAT ON (B)(6) 2009: THE PATIENT UNDERWENT FUSION SURGERY. FOLLOWING IMPLANTS WERE USED: INFUSE BONE GRAFT. MAS TERGRAFT. FLOSEAL HEMOSTATIC MATRIX (BAXTER HEALTH FOUNDATION). CRUSHED CANCELLOUS X4 (MUSCULOSKELETAL TRANSPLANT FOUNDATION)."
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 441171 | INFUSE BONE GRAFT | FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET | NEK | MEDTRONIC SOFAMOR DANEK USA, INC | NA | M110807AAJ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |