MAUDE Adverse Event Report: SYNTHES GMBH TI LCP PROXIMAL LATERAL TIBIA PL 7 HOLES/180MM-LEFT; PLATE, FIXATION, BONE

Model Number 422.223

Device Problem Use of Device Problem (1670)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 03/15/2021

Event Type  malfunction  

Manufacturer Narrative

Complainant part is not expected to be returned for manufacturer review/investigation.Without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.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 Description

Device report from synthes reports an event in (b)(6) as follows: it was reported that on (b)(6) 2021, the doctor placed a tibial implant into the distal femur.The surgery was not complicated.This report involves one (1) ti lcp proximal lateral tibia pl 7 holes/180mm-left.This is report 1 of 1 for (b)(4).

• Brand Name: TI LCP PROXIMAL LATERAL TIBIA PL 7 HOLES/180MM-LEFT
• Type of Device: PLATE, FIXATION, BONE
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): WERK HÄGENDORF (CH); im bifang 6; haegendorf 4614 ; SZ 4614
• Manufacturer Contact: kara ditty-bovard ; 1302 wright lane east; west chester, PA 19380 ; 6107195000
• MDR Report Key: 11655244
• MDR Text Key: 256234194
• Report Number: 8030965-2021-02783
• Device Sequence Number: 1
• Product Code: HRS
• UDI-Device Identifier: 10886982215086
• UDI-Public: (01)10886982215086
• Combination Product (y/n): N
• Reporter Country Code: CS
• PMA/PMN Number: K052390
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 03/15/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 422.223
• Device Catalogue Number: 422.223
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 03/15/2021
• Initial Date FDA Received: 04/13/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Age: 81 YR