MAUDE Adverse Event Report: SYNTHES RARON 3.5MM LCP RECONSTRUCTION PLATE5 HOLES/70MM; APPLIANCE,FIXATION,NAIL

Catalog Number	245.051
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(6).Date infection began is not known.Date of implant is not known.Complainant part is not expected to be returned for manufacturer review/investigation.The investigation could not be completed; no conclusion could be drawn, as no product was received.No ncrs were generated during production.Review of the device history record showed that there were no issues during the manufacture of the product that would contribute to this complaint condition.Manufacturing site: (b)(4).Manufacturing date: 03.Mar.2015.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
It was reported that a patient who initially underwent surgery for a left, tibial plateau fracture on an unknown date, was brought back to the operating room on (b)(6) 2017 for the removal of two (2) plates, twelve (12) screws and two (2) k-wires due to an infection.It is unknown when the infection was identified or if the patient had any complaints of pain or discomfort.During the procedure, the patient underwent irrigation and debridement (i and d) and the placement of a drain.It was reported that all hardware was easily removed and intact.It is unknown if the fracture was healed or if there are plans for additional surgery/treatment.The surgery was completed successfully, without delay, and the patient reported as stable.This report is for one (1) 3.5 mm lcp reconstruction plate.This is report 2 of 15 for (b)(4).

• Brand Name: 3.5MM LCP RECONSTRUCTION PLATE5 HOLES/70MM
• Common Device Name: APPLIANCE,FIXATION,NAIL
• Manufacturer (Section D): SYNTHES RARON; kanalstrasse west 30; raron CH394 2; SZ CH3942
• MDR Report Key: 6623768
• Report Number: 3006126083-2017-10023
• Device Sequence Number: 614370
• Product Code: KTT
• UDI-Device Identifier: 10886982169570
• UDI-Public: (01)10886982169570(10)9391144
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K000684
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 05/17/2017

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 Catalogue Number: 245.051
• Device Lot Number: 9391144
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/17/2017
• Initial Report FDA Received Date: 06/08/2017
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Weight: 77