BIOMET MICROFIXATION TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL; JOINT, TEMPOROMANDIBULAR, IMPLANT
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Model Number N/A |
Device Problem
Migration or Expulsion of Device (1395)
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Patient Problems
Swelling (2091); Sleep Dysfunction (2517)
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Event Type
Injury
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Manufacturer Narrative
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Zimmer biomet (b)(4).The device will not be returned for analysis as it remains implanted; however, an investigation of the reported event is in progress.Once the investigation is completed, a supplemental medwatch 3500a will be submitted.Multiple mdr reports were filed for this event, please see associated reports: 0001032347-2020-00236, 0001032347-2020-00238, 0001032347-2020-00239, 0001032347-2020-00240.Concomitant medical devices ¿ medical products: tmj system left narrow mandibular component 45 mm / 6 hole, part# 01-6546, lot# 862970c; tmj system left fossa component, small, part# 24-6563, lot# 886860c; 2.4mm system high torque (ht) cross-drive screw 2.7mm x 8mm, part# 91-2708, lot# ni; 2.4mm system high torque (ht) cross-drive screw 2.7 x 10mm, part# 91-2710, lot# ni; tmj system cross drive fossa screw 2.0mm x 7mm, part# 99-6577, lot# ni.Initial reporter ¿ patient.
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Event Description
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It was reported that the patient attended oral therapy sessions and a potentially loose screw was discovered following implantation of temporomandibular implants on the left side eleven (11) months ago.The patient reports swelling on the left side of the mouth and face, and reports difficulty sleeping on the left side.The patient attended ten oral therapy sessions to reportedly break down scar tissue, and the therapist discovered a possibly loose screw.No additional patient consequences have been reported.
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Manufacturer Narrative
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This follow-up report is being submitted to relay additional information.The complaint is considered to be confirmed because the patient received additional treatment from the oral therapist.No product was returned; therefore, no functional tests or inspections could be performed.No x-rays, scans, pictures, or physician's reports were provided.The dhr for the fossa was reviewed.Nc9780 was opened to address a label error for 24-6563.There are no indications of manufacturing defects.This is the only complaint for this item# 24-6563, lot# 886860c.For all non-custom tmj fossa implants in the previous one year (from the notification date) regarding swelling, there is a complaint rate of 0.56%, which is no greater than the occurrence listed in the application fmea.For all non-custom tmj fossa implants in the previous one year (from the notification date) regarding scar tissue, there is a complaint rate of 0.06%, which is no greater than the occurrence listed in the application fmea.For all non-custom tmj fossa implants in the previous one year (from the notification date) regarding a loose screw, there is a complaint rate of 0.28%, which is no greater than the occurrence listed in the application fmea.The most likely underlying cause of the complaint could not be determined.If any further information is found which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Event Description
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This follow-up report is being submitted to relay additional information.
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