FDA Adverse Event Injury Summary report: N

ARTICUL/EZE BALL 28 +8.5 BL

MDR report key: 4111058 · Received September 23, 2014

Report

Report Number
1818910-2014-28662
Event Type
Injury
Date Received
September 23, 2014
Date of Event
December 1, 2013
Report Date
September 12, 2014
Manufacturer
JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD. 3006356043
Product Code
JDI
PMA / PMN Number
PK883460
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PATIENT

Narratives

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. 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

NO DEVICE ASSOCIATED WITH THIS REPORT WAS RECEIVED FOR EXAMINATION. A WORLDWIDE COMPLAINT DATABASE SEARCH FOUND NO OTHER REPORTED INCIDENTS AGAINST THE PROVIDED PRODUCT/LOT COMBINATIONS SINCE RELEASE FOR DISTRIBUTION. BASED ON PREVIOUS INVESTIGATIONS THIS COMPLICATION OF JOINT REPLACEMENT IS UNLIKELY TO HAVE BEEN THE RESULT OF A DEVICE FAILING TO MEET REQUIRED SPECIFICATIONS. THE INFORMATION RECEIVED WILL BE RETAINED FOR POTENTIAL SERIES INVESTIGATIONS IF TRIGGERED BY TREND ANALYSIS, POST MARKET SURVEILLANCE, OR OTHER EVENTS WITHIN THE QUALITY SYSTEM. CORRECTIVE ACTION WAS NOT INDICATED.DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD 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 SUBMITTED COMPLAINT. PATIENT REPORTS BEING REVISED DUE TO HAVING PAIN AND LEG LENGTH ISSUES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
591565 ARTICUL/EZE BALL 28 +8.5 BL HIP FEMORAL HEAD JDI JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD. 3006356043 D11080871

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention