MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 2.7MM VA-LCP DISTAL TIBIA L-PLATE/6 HOLES/LEFT; PLATE, FIXATION, BONE

Model Number 02.118.305

Device Problem Break (1069)

Patient Problem Non-union Bone Fracture (2369)

Event Type  Injury  

Manufacturer Narrative

Additional product code: hwc.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.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

It was reported that, the patient had a tibial non-union and the tibial plate was broken.Concomitant devices reported: unknown screws (part# unknown, lot# unknown, quantity unknown).This report is for one (1) 2.7mm va-lcp distal tibia l-plate/6 holes/left.This is report 1 of 1 for (b)(4).

Manufacturer Narrative

Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If the information is unknown, not available or does not apply, the section/field of the form is left blank.Part: 02.118.305.Lot: 8762170.Manufacturing site: werk raron release to warehouse date: january 07, 2014 a manufacturing record evaluation was performed for the finished article lot and no non-conformances were identified.Product was not returned.Based on the information available, it has been determined that no corrective and 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.

• Brand Name: 2.7MM VA-LCP DISTAL TIBIA L-PLATE/6 HOLES/LEFT
• Type of Device: PLATE, FIXATION, BONE
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 12360528
• MDR Text Key: 267900335
• Report Number: 2939274-2021-04855
• Device Sequence Number: 1
• Product Code: HRS
• UDI-Device Identifier: 10886982038722
• UDI-Public: (01)10886982038722
• Combination Product (y/n): N
• PMA/PMN Number: K120854
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,health
• Type of Report: Initial,Followup
• Report Date: 07/27/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/24/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 02.118.305
• Device Catalogue Number: 02.118.305
• Device Lot Number: 8762170
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 09/01/2021
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention