FDA Adverse Event Injury Summary report: N

PINN CAN BONE SCREW 6.5MMX25MM

MDR report key: 4256167 · Received November 17, 2014

Report

Report Number
1818910-2014-31811
Event Type
Injury
Date Received
November 17, 2014
Date of Event
September 24, 2012
Report Date
April 26, 2013
Manufacturer
DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS ¿ REG.
Product Code
NDJ
PMA / PMN Number
PK983014
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
ATTORNEY

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

PPD AND MEDICAL RECORDS RECEIVED. THIS COMPLAINT IS LEGAL. PPD ALLEGES INFECTION, BUT AFTER READING THE REVISION OPERATIVE NOTE IT INDICATED PAIN, DISCOMFORT, LOOSE/MALPOSITIONED CUP, AND CYST AROUND THE GREATER TROCHANTER. EXAMINATION OF THE REPORTED DEVICES WAS NOT POSSIBLE AS THEY WERE NOT RETURNED. A SEARCH OF THE COMPLAINTS DATABASES FINDS NO OTHER REPORTS AGAINST THE PRODUCT AND LOT CODE COMBINATIONS SINCE THEIR RELEASE TO DISTRIBUTION. 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.

Description of Event or Problem · 1

PPD AND MEDICAL RECORDS RECEIVED. THIS COMPLAINT IS LEGAL. PPD ALLEGES INFECTION, BUT AFTER READING THE REVISION OPERATIVE NOTE IT INDICATED PAIN, DISCOMFORT, LOOSE/MALPOSITIONED CUP, AND CYST AROUND THE GREATER TROCHANTER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
742465 PINN CAN BONE SCREW 6.5MMX25MM HIP OTHER IMPLANT: SCREW NDJ DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS ¿ REG. 421799

Patients

Seq Age Sex Outcome Treatment
1 60 YR Required Intervention