FDA Adverse Event Injury Summary report: N

ALTRX NEUT 28IDX50OD

MDR report key: 4012120 · Received August 15, 2014

Report

Report Number
1818910-2014-25717
Event Type
Injury
Date Received
August 15, 2014
Date of Event
July 29, 2014
Report Date
July 29, 2014
Manufacturer
DEPUY ORTHOPAEDICS, INC. 1818910
Product Code
LPH
PMA / PMN Number
PK062148
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PHYSICIAN

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

EXAMINATION OF THE REPORTED DEVICES WAS NOT POSSIBLE AS THEY WERE NOT RETURNED. A SEARCH OF THE COMPLAINTS DATABASES FINDS OTHER REPORTS AGAINST THE PRODUCT AND LOT CODE COMBINATIONS. REVIEW OF DEVICE HISTORY RECORDS FINDS NO RELATED MANUFACTURING DEVIATIONS OR ANOMALIES THAT WOULD HAVE CONTRIBUTED TO THE REPORTED EVENT. ADDITIONAL EVENT INFORMATION AND INVESTIGATIONAL INPUTS WERE REQUESTED BUT NOT PROVIDED. THE INVESTIGATION CAN DRAW NO CONCLUSION WITH THE INFORMATION PROVIDED. BASED ON THE INABILITY TO DETERMINE ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION HAS NOT BEEN 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 WAS REVISED FOR DISLOCATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
490926 ALTRX NEUT 28IDX50OD HIP FEMORAL HEAD LPH DEPUY ORTHOPAEDICS, INC. 1818910 505994

Patients

Seq Age Sex Outcome Treatment
1 80 YR Required Intervention