FDA Adverse Event Injury Summary report: N

SIGMA XLK CVD PLUS INS 3 8MM

MDR report key: 4190337 · Received October 21, 2014

Report

Report Number
1818910-2014-30331
Event Type
Injury
Date Received
October 21, 2014
Date of Event
October 1, 2014
Report Date
October 1, 2014
Manufacturer
1818910 DEPUY ORTHOPAEDICS, INC.
Product Code
JWH
PMA / PMN Number
PK040166
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Additional Manufacturer Narrative · 1

THE DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO ADDITIONAL REPORTS AGAINST THE PROVIDED PRODUCT AND LOT COMBINATION. REQUESTS FOR ADDITIONAL INVESTIGATIONAL INPUTS WERE MADE IN ACCORDANCE WITH (B)(4). NO ADDITIONAL INFORMATION WAS OBTAINED. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY PRODUCT CONTRIBUTION TO THE REPORTED EVENT WITH THE INFORMATION PROVIDED. BASED ON THE INABILITY TO IDENTIFY ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Description of Event or Problem · 1

PATIENT WAS REVISED TO ADDRESS PAIN, STIFFNESS AND POOR RANGE OF MOTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
667369 SIGMA XLK CVD PLUS INS 3 8MM KNEE TIBIAL BEARING/INSERT JWH 1818910 DEPUY ORTHOPAEDICS, INC. A3VKW1

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention