ATLAS CABLE SYSTEM 826-213

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-10-17 for ATLAS CABLE SYSTEM 826-213 manufactured by Warsaw Orthopedics.

Event Text Entries

[124132614] Neither the device nor films of applicable imaging studies were returned to the manufacturer for evaluation. Therefore, we are unable to determine the definitive cause of the reported event. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[124132615] Pre-operative diagnosis: humerus fracture it was reported that intra-op, instrument was broken. Product came in contact with the patient. No fragment remained in the patient body. No patient symptoms or complication were reported during the event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1030489-2018-01363
MDR Report Key7975978
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-10-17
Date of Report2019-02-07
Date of Event2018-09-19
Date Mfgr Received2019-01-18
Device Manufacturer Date2018-03-19
Date Added to Maude2018-10-17
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 ContactSTACIE ZIEMBA
Manufacturer Street1800 PYRAMID PLACE
Manufacturer CityMEMPHIS TN 38132
Manufacturer CountryUS
Manufacturer Postal38132
Manufacturer Phone9013963133
Manufacturer G1WARSAW ORTHOPEDICS
Manufacturer Street2500 SILVEUS CROSSING
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameATLAS CABLE SYSTEM
Generic NameCABLE
Product CodeISN
Date Received2018-10-17
Returned To Mfg2019-01-09
Model NumberNA
Catalog Number826-213
Lot Number0640587W
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerWARSAW ORTHOPEDICS
Manufacturer Address2500 SILVEUS CROSSING WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-10-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.