MAUDE Adverse Event Report: DEPUY INTL., LTD.8010379 LCS COMP MOD REV FEM CEM R STD; KNEE FEMORAL COMPONENT

Catalog Number 129441040

Device Problem Loss of or Failure to Bond (1068)

Patient Problem Pain (1994)

Event Date 02/13/2014

Event Type  Injury  

Event Description

Revision due to loosening of the tibial and femoral components at the cement/implant interface and pain.Manufacturer of cement at the time of implantation is unknown.

Manufacturer Narrative

The devices associated with this report were not returned.A complaint database search finds no other reported incidents against the provided product and lot combinations.Requests for additional investigational inputs were made in accordance with wi-7915 appendix a.No additional information was obtained.The investigation could not verify or identify any product contribution to the reported event with the information provided.Based on the inability to identify root cause, the need for corrective action was not indicated.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.

Manufacturer Narrative

This complaint is still under investigation.Depuy will notify the fda of the results of this investigation once it has been completed.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: LCS COMP MOD REV FEM CEM R STD
• Type of Device: KNEE FEMORAL COMPONENT
• Manufacturer (Section D): DEPUY INTL., LTD.8010379; st. anthony's rd; leeds, leeds LS11 8 D; UK LS11 8 DT
• Manufacturer (Section G): DEPUY INTL., LTD.8010379; st. anthony's rd; leeds, leeds LS11 8 D; UK LS11 8 DT
• Manufacturer Contact: stacey trick ; 700 orthopaedic drive; warsaw, IN 46581 ; 5743714554
• MDR Report Key: 3663298
• MDR Text Key: 4344747
• Report Number: 1818910-2014-13647
• Device Sequence Number: 1
• Product Code: HRY
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: PP830055
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,Distributor
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 02/13/2014

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/06/2014
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: 129441040
• Device Lot Number: 2568755
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 03/10/2014
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 03/30/2008
• 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
• Patient Age: 65 YR