MAUDE Adverse Event Report: SMITH & NEPHEW, INC. CONT RECON RING 56/52 LFT; MESH, SURGICAL, ACETABULAR, HIP, PROSTHESIS

Catalog Number	71337156
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	07/31/2018
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported a revision surgery due to infection.Patient had recently a second revision for infection on same hip.Unfortunately the patients infection progressed leading to today's 3rd revision.Head punched off stem.Stem removed with proximal cement plug all poly cup removed with renovation instruments screws x 7 removed and contour cage removed (71337156).No lot number identifiable cage removed.Underlying mesh was overgrown by bone so left in situ.
Additional Manufacturer Narrative
The associated complaint devices were not returned.The clinical/medical team concluded, no medical documents were received for investigation.Therefore no medical assessment can be performed.A review of the production documentation for the corresponding products did not reveal any deviation from the standard manufacturing processes.Product was sterilized according to sterilization release documentation from quality control.No further clinical/medical investigation is warranted at the time.Without the actual product involved our investigation cannot proceed.If the device or new information is received in the future, this complaint can be re-opened.We consider this investigation closed.
Additional Manufacturer Narrative
Additional parts included.All of them are screws used from fixate the device already reported.

• Brand Name: CONT RECON RING 56/52 LFT
• Common Device Name: MESH, SURGICAL, ACETABULAR, HIP, PROSTHESIS
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks road; memphis TN 38116
• MDR Report Key: 7909523
• Report Number: 1020279-2018-01943
• Device Sequence Number: 13966093
• Product Code: JDH
• UDI-Device Identifier: 03596010308290
• UDI-Public: 03596010308290
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K962541
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 12/19/2018

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: 10/19/2024
• Device Catalogue Number: 71337156
• Device Lot Number: 14KM14707
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 09/03/2018
• Supplement Date Received by Manufacturer: 09/03/2018; 09/03/2018
• Initial Report FDA Received Date: 09/26/2018
• Supplement Report FDA Received Date: 09/26/2018; 12/19/2018
• 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: 71332525, 15MT62981; 71332525, 15MT62981; 71332535, 15GT56342; 71332535, 15MT62482; 71332540, 15AT49766; 71332540,15CM03345
• Outcome Attributed to Adverse Event: Hospitalization
• Patient Weight: 76