FDA Adverse Event Malfunction Summary report: N

PATH(R) THREAD CUP ADAPTOR

MDR report key: 3825202 · Received May 21, 2014

Report

Report Number
3010536692-2014-00854
Event Type
Malfunction
Date Received
May 21, 2014
Date of Event
March 27, 2014
Report Date
April 22, 2014
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
LXH
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

ALLEGEDLY AFTER IMPACTION OF THE DYNASTY CUP THE THREADED CUP ADAPTER BECAME STUCK OF THE SUPER CAP CUP IMPACTOR. PREVENTING REMOVAL OF THE SUPER PATH CUP IMPACTOR THROUGH THE DRIVE SHAFT CANNULA. (B)(6) HAS DONE A 1000 PLUS PATH PROCEDURES. THIS WAS THE SECOND TIME THIS PROBLEM OCCURRED BOTH IN THE PAST TWO WEEKS ALL USING THE NEW SUPER PATH INSTRUMENT SET.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
303280 PATH(R) THREAD CUP ADAPTOR HIP INSTRUMENT LXH MICROPORT ORTHOPEDICS INC. 1279714

Patients

Seq Age Sex Outcome Treatment
1