CANCELLOUS BONE SCREW 7552-0075

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-08-04 for CANCELLOUS BONE SCREW 7552-0075 manufactured by Microport Orthopedics Inc..

Event Text Entries

[81895752] This complaint will be updated once investigation is complete. Trends will be evaluated.
Patient Sequence No: 1, Text Type: N, H10


[81895753] Allegedly 2 most proximal screws backed out of the implant. The screws backed out screws to be removed percutaneously.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010536692-2017-01014
MDR Report Key6768784
Report SourceHEALTH PROFESSIONAL
Date Received2017-08-04
Date of Report2017-07-25
Date of Event2017-07-18
Date Facility Aware2017-07-25
Date Mfgr Received2017-07-25
Date Added to Maude2017-08-04
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 Street5677 AIRLINE ROAD
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal38002
Manufacturer Phone9018674771
Manufacturer G1MICROPORT ORTHOPEDICS INC.
Manufacturer Street5677 AIRLINE RD.
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal Code38002
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCANCELLOUS BONE SCREW
Generic NameKNEE COMPONENT
Product CodeLZN
Date Received2017-08-04
Catalog Number7552-0075
Lot Number1683003
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMICROPORT ORTHOPEDICS INC.
Manufacturer Address5677 AIRLINE RD. ARLINGTON TN 38002 US 38002


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2017-08-04

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