FDA Adverse Event Injury Summary report: N

CXD II

MDR report key: 1894801 · Received November 10, 2010

Report

Report Number
1423500-2010-05559
Event Type
Injury
Date Received
November 10, 2010
Date of Event
September 1, 2010
Report Date
October 18, 2010
Manufacturer
BAXTER HEALTHCARE - LARGO
Product Code
KDJ
PMA / PMN Number
K851208
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CT, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4) - AS THE DATE OF ONSET OF THIS PERITONITIS EPISODE IS UNKNOWN THE SAMPLE WAS NOT REQUESTED.

Additional Manufacturer Narrative · 1

(B)(4). BAXTER HAS RECEIVED SIMILAR REPORTS. THE ROOT CAUSE INVESTIGATION IS IN PROGRESS.

Description of Event or Problem · 1

PT WAS REVISED TO ADDRESS LOOSENING OF THE TIBIAL TRAY AND FEMORAL COMPONENT AT THE CEMENT/BONE INTERFACE (CEMENT MANUFACTURER UNK). OSTEOLYSIS AND POLY WEAR OF THE INSERT WERE ALSO REPORTED. ALSO, DURING THIS SURGERY, A TC3 RP SZ 5 17.5 MM INSERT WAS IMPLANTED WITH A SZ 5 LEFT C/S FEMUR. THE SURGEON WAS MADE AWARE OF THIS AFTER THE PT WAS REMOVED FROM ROOM. SURGEON DID NOT NOTICE ANY ADVERSE MECHANICAL EFFECTS WHILE PUTTING THE KNEE THROUGH A RANGE OF MOTION, SO HE DECIDED TO LEAVE THE MISMATCHED COMPONENTS IN.

Description of Event or Problem · 1

DURING FOLLOW-UP FOR AN UNRELATED ALARM, THE PATIENT INDICATED SHE HAD PERITONITIS. FOLLOW-UP INFORMATION OBTAINED IS AS FOLLOWS: THE CAUSE OF THE PERITONITIS IS UNKNOWN AND THE PATIENT HAS RECOVERED FROM THE PERITONITIS. THE PATIENT IS CURRENTLY ON HEMODIALYSIS. THE NURSE DECLINED TO PROVIDE ANY ADDITIONAL INFORMATION REGARDING THE PERITONITIS, ONLY INDICATING THAT THE DATE OF DIAGNOSIS WAS (B)(6) 2010 AND THAT THE PATIENT'S TRANSFER SET WAS REPLACED AFTER THE DIAGNOSIS. NO FURTHER INFORMATION WILL BE PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CXD II SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE KDJ BAXTER HEALTHCARE - LARGO

Patients

Seq Age Sex Outcome Treatment
1 33 YR Required Intervention