GPS MINI KIT W /ACD-A & BD N/A 800-0670A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2014-08-25 for GPS MINI KIT W /ACD-A & BD N/A 800-0670A manufactured by Biomet Orthopedics.

Event Text Entries

[4842276] It was reported patient underwent a lateral epicondylitis inflammation procedure on (b)(6) 2014. During the procedure, the gps component would not fill with blood. Subsequently, the procedure was abandoned and could not be completed.
Patient Sequence No: 1, Text Type: D, B5


[12276303] Current information is insufficient to permit a conclusion as to the cause of the event. Review of device history records show that lot released with no recorded anomaly or deviation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number0001825034-2014-07256
MDR Report Key4034055
Report Source01,05
Date Received2014-08-25
Date of Report2014-08-14
Date of Event2014-04-24
Date Mfgr Received2014-08-14
Device Manufacturer Date2014-03-07
Date Added to Maude2014-09-08
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 FDA0
Event Location0
Manufacturer ContactMS. MEGAN HAAS
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5743726700
Manufacturer G1BIOMET ORTHOPEDICS
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameGPS MINI KIT W /ACD-A & BD
Generic NameSUPPLIES, BLOOD BANK
Product CodeKSS
Date Received2014-08-25
Model NumberN/A
Catalog Number800-0670A
Lot Number400524
ID NumberN/A
Device Expiration Date2016-10-31
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET ORTHOPEDICS
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
10 2014-08-25

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