FDA Adverse Event Injury Summary report: N

UNKNOWN DEPUY SZ. 32 +5 FEMORAL HEAD

MDR report key: 6064346 · Received October 28, 2016

Report

Report Number
1818910-2016-30339
Event Type
Injury
Date Received
October 28, 2016
Date of Event
October 18, 2016
Report Date
October 18, 2016
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
JDG
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, 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. DEPUY SYNTHES HAS BEEN INFORMED THAT THE CATALOG NUMBER AND LOT NUMBER IS NOT AVAILABLE.

Additional Manufacturer Narrative · 1

PATIENT WAS REVISED TO ADDRESS A DISLOCATION. IT WAS ALSO NOTED THAT THE PATIENT'S PELVIC RAMUS WAS FRACTURED. IT IS UNKNOWN WHEN THE FRACTURE OCCURRED. EXAMINATION OF THE REPORTED DEVICE WAS NOT POSSIBLE AS IT WAS NOT RETURNED. A SEARCH OF THE COMPLAINTS DATABASES AND/OR A REVIEW OF DEVICE HISTORY RECORDS WERE NOT POSSIBLE AS THE REQUIRED PRODUCT/LOT CODE COMBINATION WAS NOT PROVIDED. THE INVESTIGATION CAN DRAW NO CONCLUSION REGARDING THE REPORTED EVENT WITH THE INFORMATION AVAILABLE. BASED ON THE INABILITY TO DETERMINE ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION HAS NOT BEEN INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED THE INVESTIGATION WILL BE REOPENED.

Description of Event or Problem · 1

PATIENT WAS REVISED TO ADDRESS A DISLOCATION. IT WAS ALSO NOTED THAT THE PATIENT'S PELVIC RAMUS WAS FRACTURED. IT IS UNKNOWN WHEN THE FRACTURE OCCURRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
715274 UNKNOWN DEPUY SZ. 32 +5 FEMORAL HEAD HIP FEMORAL HEAD JDG DEPUY ORTHOPAEDICS, INC. UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention