FDA Adverse Event Injury Summary report: N

SROM*STM LG 36+8L 22X17X230N

MDR report key: 2950488 · Received February 8, 2013

Report

Report Number
1818910-2013-12047
Event Type
Injury
Date Received
February 8, 2013
Date of Event
January 25, 2013
Report Date
January 25, 2013
Manufacturer
DEPUY (IRELAND)
Product Code
JDI
PMA / PMN Number
PK851422
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PATIENT WAS REVISED TO ADDRESS PAIN AND LOOSENING OF THE SLEEVE AND STEM. SURGEON QUESTIONS BONE QUALITY AND SLIGHT UNDER-SIZING OF IMPLANTS, WHICH LED TO THE LOOSENING. DOI (B)(6) 2006 - 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. PER FOLLOW UP; PATIENT X-RAYS ARE NOT AVAILABLE FOR EXAMINATION. 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 AND LOOSENING OF THE SLEEVE AND STEM. SURGEON QUESTIONS BONE QUALITY AND SLIGHT UNDERSIZING OF IMPLANTS, WHICH LED TO THE LOOSENING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
53742 SROM*STM LG 36+8L 22X17X230N FEMORAL HIP STEM JDI DEPUY (IRELAND) 1830316

Patients

Seq Age Sex Outcome Treatment
1 77 YR Required Intervention