FDA Adverse Event Malfunction Summary report: N

PATH(R) THREAD CUP ADAPTOR

MDR report key: 3827975 · Received May 22, 2014

Report

Report Number
3010536692-2014-00860
Event Type
Malfunction
Date Received
May 22, 2014
Date of Event
March 28, 2014
Report Date
April 22, 2014
Manufacturer
MICROPORT ORTHOPEDICS INC.
Product Code
KWA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

ALLEGEDLY THE ADAPTOR STICKS WITH THE HANDLE. HAPPENED IN LAB.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
304745 PATH(R) THREAD CUP ADAPTOR HIP INSTRUMENT KWA MICROPORT ORTHOPEDICS INC. NI

Patients

Seq Age Sex Outcome Treatment
1