MAUDE Adverse Event Report: ENCORE MEDICAL, L.P. FMP HIP; HEAD, FEMORAL, COCR 28/+10.5MM

Catalog Number	497-28-105
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	11/17/2016
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - due to poor post-operation treatment/care; resulting in an infection.
Additional Manufacturer Narrative
The reason for this revision surgery was an infection.The previous surgery and the revision detailed in this investigation occurred 20 days apart.The healthcare professional indicated there was no delay in surgery and another suitable device was available for use.The revision surgery was completed as intended.The device was disposed of at the hospital and not made available to djo surgical for examination.A review of the implant device history records (dhrs) show that the reported component used in the previous surgery met design and manufacturing requirements.There were no non-conforming material reports (ncmrs) associated with the product that may have contributed to an infection.The device was verified to have gone through an acceptable sterilization process and was within it's expiration date at the time of use during the previous surgery.There were no findings during this investigation that indicate that the reported device was the root cause or had a direct connection with the patient's infection.The complaint reported that poor post-operation treatment/care was the root cause of the infection.There are multiple factors that may contribute to an infection that are outside of the control of djo surgical.There are no indications of a product or process issue affecting implant safety or effectiveness.

• Brand Name: FMP HIP
• Common Device Name: HEAD, FEMORAL, COCR 28/+10.5MM
• Manufacturer (Section D): ENCORE MEDICAL, L.P.; 9800 metric blvd.; austin TX 78758
• MDR Report Key: 6183402
• Report Number: 1644408-2016-00983
• Device Sequence Number: 13716494
• Product Code: JDI
• UDI-Device Identifier: 00888912087285
• UDI-Public: (01)00888912087285
• Combination Product (Y/N): N
• Initial Reporter State: MS
• Initial Reporter Country: US
• PMA/510(K) Number: K932481
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2016
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 01/19/2017

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
• Operator of Device: Health Professional
• Device Expiration Date: 01/20/2022
• Device Catalogue Number: 497-28-105
• Device Lot Number: 632C1131
• Was Device Available for Evaluation?: No
• Type of Report(Section G): FDA Requested
• Initial Date Received by Manufacturer: 11/17/2016
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 12/16/2016
• Supplement Report FDA Received Date: 01/19/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 436-28-000,LOT 496C1063; 436-28-011,LOT 503C1009
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 84 YR