FDA Adverse Event Injury Summary report: N

INFUSE BONE GRAFT

MDR report key: 3193412 · Received June 27, 2013

Report

Report Number
1030489-2013-02602
Event Type
Injury
Date Received
June 27, 2013
Report Date
October 24, 2016
Manufacturer
MEDTRONIC SOFAMOR DANEK USA, INC
Product Code
NEK
PMA / PMN Number
P000058
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

(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.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT A LATERAL FUSION AT L1-L2-L3 AND AT L5-S1 USING RHBMP-2/ACS. POSTOPERATIVELY, PATIENT DEVELOPED AN EPIDURAL ABSCESS, NECESSITATING DEBRIDEMENT AND IV ANTIBIOTICS. FOLLOW-UP RECORDS REPORTEDLY INDICATE THAT THE PATIENT CONTINUED TO EXPERIENCE SIGNIFICANT LEFT LEG PAIN. A CT SCAN REPORTEDLY INDICATED FORAMINAL ENCROACHMENT ON THE LEFT SIDE AT L3-4 AND L4-5 WITH BONY OVERGROWTH. AS A RESULT, THE PATIENT HAS REQUIRED EXTENSIVE MEDICAL TREATMENT AND CONTINUES TO SUFFER FROM DAILY, DEBILITATING PAIN. THE PATIENT HAS NEVER RECOVERED FROM HER SURGERY INVOLVING BMP, AND SHE CONTINUES TO HAVE DAILY SEVERE DISABLING PAIN THAT PREVENTS HER FROM PERFORMING MANY BASIC ACTIVITIES OF DAILY LIVING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
293863 INFUSE BONE GRAFT FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET NEK MEDTRONIC SOFAMOR DANEK USA, INC NA UNK

Patients

Seq Age Sex Outcome Treatment
1 00063 YR Required Intervention