FDA Adverse Event Injury Summary report: N

INFUSE BONE GRAFT

MDR report key: 1841298 · Received September 13, 2010

Report

Report Number
1030489-2010-01184
Event Type
Injury
Date Received
September 13, 2010
Date of Event
February 17, 2006
Report Date
August 16, 2010
Manufacturer
MEDTRONIC SOFAMOR DANEK USA, INC.
Product Code
NEK
PMA / PMN Number
P000058
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). LITERATURE CITATION: SMUCKER, ET AL. INCREASED SWELLING COMPLICATIONS ASSOCIATED WITH OFF-LABEL USAGE OF RHBMP-2 IN THE ANTERIOR CERVICAL SPINE. SPINE. 2006; VOLUME 31, NUMBER 24: PP 2813-2819. A REVIEW OF THE DEVICE HISTORY RECORDS CANNOT BE PERFORMED WITHOUT ADDITIONAL DEVICE INFORMATION. WITHOUT RETURN OF THE DEVICE OR ASSOCIATED RECORDS, IT IS NOT POSSIBLE TO ASCERTAIN A CAUSE FOR THE REPORTED EVENT.

Description of Event or Problem · 1

SWELLING COMPLICATIONS WERE REPORTED IN A RETROSPECTIVE STUDY OF PTS WHO UNDERWENT ANTERIOR CERVICAL FUSION USING RHBMP-2. FUSION WAS PERFORMED THROUGH A STANDARD SURGICAL APPROACH USING RHBMP-2 AT A CONCENTRATION OF 1.5MG/ML, HOWEVER THE ACTUAL DOSE OF RHBMP-2 APPLIED COULD NOT BE DETERMINED. IN THIS PT, IT IS NOT KNOWN IF RHBMP-2 WAS PLACED IN A CORTICAL RING ALLOGRAFT OR INTERBODY SPACER, AND/OR AROUND THE GRAFT ITSELF IN THE DISC SPACE. THE SWELLING COMPLICATION OCCURRED IN A DELAYED FASHION AFTER A SEEMINGLY UNEVENTFUL SURGERY, EXTUBATION, AND INITIAL POSTOPERATIVE COURSE. THREE DAYS POST OPERATIVELY, THIS PT WHO UNDERWENT AN INITIAL 2-LEVEL ANTERIOR CERVICAL FUSION WAS READMITTED TO THE HOSPITAL FOR OBSERVATION AND MEDICAL MANAGEMENT OF SWELLING. NO OTHER DETAILS OR OUTCOMES WERE MENTIONED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INFUSE BONE GRAFT INFUSE BONE GRAFT NEK MEDTRONIC SOFAMOR DANEK USA, INC. NA UNK

Patients

Seq Age Sex Outcome Treatment
1 UNK Hospitalization