MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 3.5MM LCP LOW BEND MEDIAL DSTL TIBIA PLATE/8H/RIGHT/161MM; PLATE, FIXATION, BONE

Model Number	02.112.518
Medical Device Problem Code	Device-Device Incompatibility (2919)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/14/2021
Type of Reportable Event	Malfunction
Additional 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 or Problem Description
It was reported that on (b)(6) 2021 while inserting a distal tibia plate, the aiming arm was missing the proximal holes.After the case it was determined that there was an issue with the aiming arm and it is possible that the right side aiming arm was either damaged/bent.Once the problem was identified, the surgery proceeded and was successfully finished.The surgery was delayed for 15 minutes.This report is for one (1) 3.5mm lcp low bend medial dstl tibia plate/8h/right/161mm.This is report 3 of 3 for complaint for (b)(4).

• Brand Name: 3.5MM LCP LOW BEND MEDIAL DSTL TIBIA PLATE/8H/RIGHT/161MM
• Common Device Name: PLATE, FIXATION, BONE
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 11477500
• Report Number: 2939274-2021-01307
• Device Sequence Number: 17154018
• Product Code: HRS
• UDI-Device Identifier: 10886982034557
• UDI-Public: (01)10886982034557
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K013248
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 02/14/2021

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
• Operator of Device: Health Professional
• Device Model Number: 02.112.518
• Device Catalogue Number: 02.112.518
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/14/2021
• Initial Report FDA Received Date: 03/12/2021
• Patient Sequence Number: 1
• Patient Age: 66 YR
• Patient Weight: 98