SAFSITE ACCESS PIN AP-2500

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-07-18 for SAFSITE ACCESS PIN AP-2500 manufactured by Burron Medical Inc..

Event Text Entries

[20160578] Safsite access pin found to be defective; failed to puncture. No injury/harm to patient occurred. Report submitted to fda and usp. Invalid data - regarding single use labeling of device. Patient medical status prior to event: invalid data. Invalid data - regarding multiple patient involvement. Invalid data - on device service/maintenance. No data - regarding date last serviced. Service provided by: invalid data. Invalid data - service records availability. Invalid data - regarding whether event presents imminent hazard. Invalid data - whether device used as labeled/intended. Invalid data - regarding evaluation by user after event. Method of evaluation: invalid data. Results of evaluation: invalid data. Conclusion: invalid data. Certainty of device as cause of or contributor to event: invalid data. Corrective actions: no data. Invalid data - on device destroyed/disposed of status.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9413
MDR Report Key9413
Date Received1994-07-18
Date of Report1994-07-06
Report Date1994-07-06
Date Added to Maude1994-12-12
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameSAFSITE ACCESS PIN AP-2500
Product CodeEBL
Date Received1994-07-18
ID NumberAP-2500
Device Availability*
Implant Flag*
Device Sequence No1
Device Event Key9070
ManufacturerBURRON MEDICAL INC.


Patients

Patient NumberTreatmentOutcomeDate
101. No Informationnvalid Deathata 1994-07-18

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