FDA Adverse Event Injury Summary report: N

LORENZ TITANIUM FRACTURE / RECONSTRUCTION PLATING

MDR report key: 5870086 · Received August 11, 2016

Report

Report Number
0001032347-2016-00397
Event Type
Injury
Date Received
August 11, 2016
Date of Event
July 1, 2016
Report Date
July 13, 2016
Manufacturer
BIOMET MICROFIXATION
Product Code
HWC
PMA / PMN Number
PK001238
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THE PRODUCT WAS NOT RETURNED FOR AN EVALUATION, HOWEVER AN EVALUATION OF THE COMPLAINT WAS CONDUCTED. THIS IS REPORT THREE OF FIVE FOR THE SAME EVENT. REPORTS ONE, TWO, FOUR, AND FIVE ARE REPORTED ON 1032347-2016-00395-1, 1032347-2016-00396-1, 1032347-2016-00398-1, AND 1032347-2016-00399-1.

Additional Manufacturer Narrative · 1

IT WAS REPORTED THE PATIENT IS IN IN JAIL AND THE SURGEON BELIEVES THE EVENT WAS DUE TO THE PATIENT NOT HAVING ACCESS TO ORAL CARE. THE LOT NUMBER IS UNKNOWN; THEREFORE THE DEVICE HISTORY RECORDS ARE UNABLE TO BE REVIEWED. THE WARNINGS IN THE PACKAGE INSERT STATE THIS TYPE OF EVENT CAN OCCUR. IF ADDITIONAL INFORMATION IS OBTAINED THAT ADDS VALUE TO THE RELEVANT CONTENT OF THIS REPORT A FOLLOW-UP REPORT WILL BE SENT. REPORT THREE OF FIVE FOR THE SAME EVENT, REFERENCE 1032347-2016-00395 THROUGH 1032347-2016-00399.

Description of Event or Problem · 1

IT WAS REPORTED THAT ALL PREVIOUSLY IMPLANTED PRODUCTS WERE RE-IMPLANTED INTO THE PATIENT ONCE THE PATIENT'S CONDITION WAS RESOLVED.

Description of Event or Problem · 1

A REVISION SURGERY WAS REPORTED DUE TO ANKYLOSIS OVER THE JOINT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
522524 LORENZ TITANIUM FRACTURE / RECONSTRUCTION PLATING 2.7X10MM HT X-DRIVE SCREW HWC BIOMET MICROFIXATION N/A UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R