UNKNOWN BIOMET SCREW

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-02-11 for UNKNOWN BIOMET SCREW manufactured by Biomet 3i.

Event Text Entries

[178565023] Zimmer biomet complaint number (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[178565024] It was reported that the screw that goes from the crown to the implant head has fractured. An attempt was made to remove the screw but it was seized. The implant fos413 in dental site 30 was removed with trephine.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001038806-2020-00310
MDR Report Key9691482
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-02-11
Date of Report2020-02-11
Date of Event2020-01-02
Date Mfgr Received2020-01-16
Date Added to Maude2020-02-11
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS SUSANNE TAYLOR
Manufacturer Street4555 RIVERSIDE DRIVE
Manufacturer CityPALM BEACH GARDENS FL 33410
Manufacturer CountryUS
Manufacturer Postal33410
Manufacturer Phone5617766700
Manufacturer G1BIOMET 3I
Manufacturer Street4555 RIVERSIDE DRIVE
Manufacturer CityPALM BEACH GARDENS FL 33410
Manufacturer CountryUS
Manufacturer Postal Code33410
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Generic NameDENTAL SCREW
Product CodeDZL
Date Received2020-02-11
Catalog NumberUNKNOWN BIOMET SCREW
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET 3I
Manufacturer Address4555 RIVERSIDE DRIVE PALM BEACH GARDENS FL 33410 US 33410


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-11

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