FDA Adverse Event Injury Summary report: N

INFUSE BONE GRAFT X-SMALL KIT

MDR report key: 1730085 · Received June 18, 2010

Report

Report Number
1030489-2010-00819
Event Type
Injury
Date Received
June 18, 2010
Date of Event
December 5, 2009
Report Date
May 25, 2010
Manufacturer
MEDTRONIC SOFAMOR DANEK USA, INC.
Product Code
NEK
PMA / PMN Number
P000058
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B) (4). LITERATURE CITATION: GARRETT ET AL, "FORMATION OF PAINFUL SEROMA AND EDEMA AFTER THE USE OF RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2 IN POSTEROLATERAL LUMBAR SPINE FUSIONS" IN NEUROSURGERY (2010; 66: 1044-1049). NEITHER THE DEVICE NOR APPLICABLE IMAGING FILMS WERE RETURNED TO THE MANUFACTURER FOR EVAL. A REVIEW OF THE DEVICE HISTORY RECORDS IS NOT POSSIBLE WITHOUT ADDITIONAL DEVICE INFO. THEREFORE, THE CAUSE OF THE EVENT CANNOT BE DETERMINED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PT UNDERWENT A L4-L5 POSTERIOR LUMBAR INTERBODY FUSION/POSTEROLATERAL SPINAL FUSION USING RHBMP-2/ACS PLUS POSTERIOR FIXATION. AT AN UNK TIME POST-OP, THE PT PRESENTED WITH SEVERE PAIN, SWELLING, ERYTHEMA AND TENDERNESS TO PALPATION AT THE SURGICAL SITE. SIX DAYS POST-OP, THE PT UNDERWENT AN EXPLORATORY SURGERY FOR POTENTIAL INFECTION AND TO DECOMPRESS THE SWELLING AT THE SURGICAL SITE. INFECTION WAS RULED OUT WITH INTRAOPERATIVE CULTURES. THE SUBCUTANEOUS TISSUES WERE EDEMATOUS AND NOTED TO BE "SEEPING" WHEN THE RETRACTORS WERE PLACED. AN EPI/SUBFASCIAL SEROMA WAS ENCOUNTERED AND DRAINED. THE SEROMA DID NOT RE-FORM AFTER THE SECOND SURGERY.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 34 YR Hospitalization| R TITANIUM PEDICLE SCREWS