1.5 MM SYSTEM HIGH TORQUE (HT), SD, X-DR, SCR, 5-PK, 1.5 X 5 MM N/A 95-6105

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-12 for 1.5 MM SYSTEM HIGH TORQUE (HT), SD, X-DR, SCR, 5-PK, 1.5 X 5 MM N/A 95-6105 manufactured by Biomet Microfixation.

Event Text Entries

[130168793] Zimmer biomet complaint (b)(4), (b)(4), foreign country: (b)(6). Customer has indicated that the product is in process of being returned to zimmer biomet for investigation. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[130168794] It was reported the screws fractured during surgery. The procedure was completed with another screw of the same size. It is stated the surgical technique was not followed. Attempts have been made and no further information has been provided. No additional patient consequences were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001032347-2018-00855
MDR Report Key8157422
Date Received2018-12-12
Date of Report2019-01-31
Date of Event2018-07-04
Date Mfgr Received2018-12-19
Device Manufacturer Date2017-10-20
Date Added to Maude2018-12-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. MICHELLE COLE
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal32218
Manufacturer Phone9047414400
Manufacturer G1BIOMET MICROFIXATION
Manufacturer Street1520 TRADEPORT DRIVE
Manufacturer CityJACKSONVILLE FL 32218
Manufacturer CountryUS
Manufacturer Postal Code32218
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand Name1.5 MM SYSTEM HIGH TORQUE (HT), SD, X-DR, SCR, 5-PK, 1.5 X 5 MM
Generic NameFASTENER, SCREW, CRANIOPLASTY
Product CodeGWO
Date Received2018-12-12
Model NumberN/A
Catalog Number95-6105
Lot Number756820
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET MICROFIXATION
Manufacturer Address1520 TRADEPORT DRIVE JACKSONVILLE FL 32218 US 32218


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-12-12

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