FDA Adverse Event Injury Summary report: N

TOTAL HIP BALL 32MM +0

MDR report key: 1983454 · Received January 31, 2011

Report

Report Number
1818910-2011-00098
Event Type
Injury
Date Received
January 31, 2011
Date of Event
December 1, 2010
Report Date
January 5, 2011
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
JDI
PMA / PMN Number
K880269
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

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.

Additional Manufacturer Narrative · 1

JOHNSON AND JOHNSON MEDICAL (B)(6) REPORTS: REVISION RIGHT AML / DURALOC TOTAL HIP REPLACEMENT. PRIMARY SURGERY IN 1993 AT (B)(6) HOSPITAL. LINER/ DURALOC SCREW 35MM AND HEAD REMOVED. CUP REMAINED SECURE INSITU, NEW SCREWS 6.5 MM INSERTED LENGTHS 30 MM AND 40 MM ALSO 62MM LOCKING RING AND DURALOC MARATHON LINER 32MMID 10 DEGREE LIPPED INSERTED. A 32MM HEAD +0. THE DEVISES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. A SEARCH OF THE COMPLAINT DATABASE DID NOT SHOW ANY OTHER REPORTS AGAINST THE PRODUCT AND LOT COMBINATION. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT WITH THE INFORMATION AVAILABLE. 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 AND / OR ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.

Description of Event or Problem · 1

PT WAS REVISED TO ADDRESS PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTAL HIP BALL 32MM +0 87JDI JDI DEPUY ORTHOPAEDICS, INC. NA 586990011

Patients

Seq Age Sex Outcome Treatment
1 NA Required Intervention