MAUDE Adverse Event Report: SMITH & NEPHEW, INC. MTX CEMENTED CUP X BAR; PROSTHESISHIPSEMI-CONSTRAINEDMETAL/METALRESURFACING

Model Number MT2201

Device Problem Break (1069)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 01/20/2020

Event Type  malfunction  

Event Description

It was reported that during surgery, the x bar welding was no longer welded and the head trial is cracked inside.Smith&nephew backup device was available.The device malfunctioned within the patient.All pieces were retrieved.No delay.No injury to patient.

Manufacturer Narrative

The devices, used in treatment were not returned for evaluation, reporting event could not be confirmed.A complaint history review found related failures; this failure mode will be monitored for future complaints for any necessary corrective actions.This device is a reusable instrument that can be exposed to numerous surgeries; damage from repeated use can occur.Damage from prolonged use, misuse or rough handling are likely probable causes of the reported event.We recommend that all reusable instruments be routinely inspected for wear and damage and replaced as necessary.At this time, we have no reason to suspect that the product failed to meet any product specifications at the time of manufacture.Based on this investigation, the need for corrective action is not indicated.Without the actual product involved and/or device information, our investigation cannot proceed.If the device or new information is received in the future, this complaint can be re-opened.No further actions are being taken at this time.

• Brand Name: MTX CEMENTED CUP X BAR
• Type of Device: PROSTHESISHIPSEMI-CONSTRAINEDMETAL/METALRESURFACING
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks road; memphis TN 38116
• MDR Report Key: 9720227
• MDR Text Key: 182341099
• Report Number: 1020279-2020-00601
• Device Sequence Number: 1
• Product Code: NXT
• UDI-Device Identifier: 03596010012302
• UDI-Public: 03596010012302
• Combination Product (y/n): N
• PMA/PMN Number: P040033
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Type of Report: Initial,Followup
• Report Date: 03/26/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/18/2020
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: MT2201
• Device Catalogue Number: ORMT2201
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 03/19/2020
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1