FDA Adverse Event Malfunction Summary report: N

ATTUNE SPACER BLOCK

MDR report key: 6131408 · Received November 29, 2016

Report

Report Number
1818910-2016-32339
Event Type
Malfunction
Date Received
November 29, 2016
Date of Event
November 8, 2016
Report Date
November 8, 2016
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
HWT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
HEALTH PROFESSIONAL

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. UDI: (B)(4).

Additional Manufacturer Narrative · 1

THE COMPLAINT STATES THE SPRING BROKE OFF THE SPACER BLOCK. THE INVESTIGATION CONFIRMED THE FAILURE MODE AS REPORTED. CARE NEEDS TO BE USED WHEN ASSEMBLING THESE CONNECTIONS, AS DAMAGE MAY OCCUR RESULTING IN THE TYPE OF FAILURE SEEN HERE. HOWEVER, THERE IS INSUFFICIENT INFORMATION SUPPLIED WITH THIS COMPLAINT TO DETERMINE WHETHER SUFFICIENT CARE WAS OR WAS NOT TAKEN. IT SHOULD BE NOTED THAT PRA (B)(4) WAS RELEASED ON 08 JUL 2014 IN WHICH THE DAMAGE TO THE BALSEALS WAS EVALUATED. THE PRA CONCLUDED THAT THERE IS NO PATIENT HARM AS NONE OF THE FAILURE MODES HAVE LED TO ANY PATIENT HARM. FURTHERMORE, THE ASSEMBLY AND DISASSEMBLY OF THIS DEVICE IS CARRIED OUT BY THE SCRUB NURSE ON A TABLE AWAY FROM THE JOINT SPACE, ADDITIONALLY THE DEVICE CANNOT BE DISASSEMBLED WITHIN THE JOINT SPACE. IT SHOULD ALSO BE NOTED THAT THIS ISSUE WILL BE FURTHER MONITORED IN POST MARKET SURVEILLANCE THE COMPLAINT SHALL BE CLOSED WITH AN UNDETERMINED CONCLUSION AND ENTERED INTO THE COMPLAINTS SYSTEM AND MONITORED THROUGH TREND ANALYSIS. IF FURTHER INFORMATION IS RECEIVED THE COMPLAINT SHALL BE REOPENED AND INVESTIGATED FURTHER. 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

THE SPRING BROKE OFF THE SPACER BLOCK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
783164 ATTUNE SPACER BLOCK KNEE INSTRUMENT/TRIAL HWT DEPUY ORTHOPAEDICS, INC. BFA0N7C

Patients

Seq Age Sex Outcome Treatment
1