FDA Adverse Event Injury Summary report: N

S-ROM M HEAD 36MM +3

MDR report key: 2934351 · Received January 30, 2013

Report

Report Number
1818910-2013-11645
Event Type
Injury
Date Received
January 30, 2013
Date of Event
January 22, 2013
Report Date
January 22, 2013
Manufacturer
DEPUY ORTHOPAEDICS INC US
Product Code
JDI
PMA / PMN Number
PK851422
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS COMPLAINT IS CONSIDERED CLOSED.

Additional Manufacturer Narrative · 1

PATIENT WAS REVISED TO ADDRESS PAIN. DOI (B)(6) 2009 - DOR (B)(6) 2013 (LEFT HIP). THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO OTHER REPORTED INCIDENTS AGAINST THE PROVIDED PRODUCT AND LOT COMBINATIONS SINCE THEIR RELEASE FOR DISTRIBUTION. FOLLOW UP WAS PERFORMED FOR ADDITIONAL INVESTIGATIVE IN-PUTS BUT NO ADDITIONAL INFORMATION WAS OBTAINED. NO ADDITIONAL INFORMATION WAS OBTAINED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT. BASED ON THE INABILITY TO DETERMINE A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT OR ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.

Additional Manufacturer Narrative · 1

THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

Description of Event or Problem · 1

PATIENT WAS REVISED TO ADDRESS PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
40625 S-ROM M HEAD 36MM +3 FEMORAL HEAD JDI DEPUY ORTHOPAEDICS INC US 2773004

Patients

Seq Age Sex Outcome Treatment
1 51 YR Required Intervention