FDA Adverse Event Injury Summary report: N

INFUSE BONE GRAFT

MDR report key: 2830055 · Received November 13, 2012

Report

Report Number: 1030489-2012-02113
Event Type: Injury
Date Received: November 13, 2012
Report Date: February 9, 2018
Manufacturer: MEDTRONIC SOFAMOR DANEK USA, INC
Product Code: NEK
PMA / PMN Number: P000058
Adverse Event: Yes
Report Source: Manufacturer report
Reporter Location: CA, US
Reporter Occupation: ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

DATE OF IMPLANT: (B)(6) 2008. (B)(6). (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

(B)(4)

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

REPORTEDLY THE PATIENT DEVELOPED "... SIGNFICIANT PROBLEMS) AS WELL AS PAIN, MENTAL ANGUISH, PHYSICAL LIMITATIONS, AND A NEED TO UNDERGO A REVISION SURGERY."

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT SUSTAINED UNSPECIFIED INJURIES FOLLOWING THE USE OF RHBMP-2/ACS IN AN UNSPECIFIED SPINAL FUSION SURGERY. NO ADDITIONAL INFORMATION WAS REPORTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT ON (B)(6) 2008, THE PATIENT UNDERWENT L2-L3 DECOMPRESSION L3-S1 HARDWARE REMOVAL, EXPLORE FUSION, L2-L3 FUSION, POSS. L3-S1, RHBMP-2, INSTRUMENTATION IN WHICH RHBMP-2/ACS WAS USED.

Devices

Seq	Brand	Generic	Product Code	Manufacturer	Model	Lot	UDI-DI
1	INFUSE BONE GRAFT	FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET	NEK	MEDTRONIC SOFAMOR DANEK USA, INC	NA	M110709AAJ

Patients

Seq	Age	Sex	Outcome	Treatment
1			Other\| R