MAUDE Adverse Event Report: EXACTECH, INC NOVATION FEMORAL STEM, TAPERED, 12/14, EXTENDED OFFSET, PLASMA COATED, PRESS-FIT

Catalog Number 160-01-16

Device Problem Device Dislodged or Dislocated (2923)

Patient Problem Pain (1994)

Event Date 06/01/2012

Event Type  malfunction  

Manufacturer Narrative

The contribution of the devices to the experience reported could not be determined as the devices were not returned for evaluation.Additionally, the device specific information was not provided, precluding a review of the device history record.

Event Description

Index surgery: (b)(6) 2012.On (b)(6), patient crossed legs and developed acute right hip pain.Surgeon performed closed reduction.On (b)(6), patient dislocated when getting up from a table.On (b)(6), patient dislocated again and surgeon performed closed reduction.This event report was received through clinical data collection activities.

• Brand Name: NOVATION FEMORAL STEM, TAPERED, 12/14, EXTENDED OFFSET, PLASMA COATED, PRESS-FIT
• Type of Device: FEMORAL STEM
• Manufacturer (Section D): EXACTECH, INC; 2320 nw 66th ct; gainesville FL 32653
• Manufacturer (Section G): EXACTECH, INC; 2320 nw 66th ct; gainesville FL 32653
• Manufacturer Contact: graham cuthbert ; 2320 nw 66th ct; gainesville, FL 32653 ; 3523771140
• MDR Report Key: 5334234
• MDR Text Key: 35101062
• Report Number: 1038671-2015-00726
• Device Sequence Number: 1
• Product Code: MRA
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 12/30/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Physician
• Device Catalogue Number: 160-01-16
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 12/09/2015
• Initial Date FDA Received: 12/30/2015
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention