BASIC MAGNETIC PULL-CORD ALARM 74836

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-20 for BASIC MAGNETIC PULL-CORD ALARM 74836 manufactured by Alimed Inc.

MAUDE Entry Details

Report Number7633544
MDR Report Key7633544
Date Received2018-06-20
Date of Report2018-06-20
Date of Event2018-06-08
Date Facility Aware2018-06-08
Report Date2018-06-20
Date Reported to FDA2018-06-20
Date Reported to Mfgr2018-06-20
Date Added to Maude2018-06-25
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBASIC MAGNETIC PULL-CORD ALARM
Generic NameMAGNETIC ALARM
Product CodeKMI
Date Received2018-06-20
Model Number74836
OperatorLAY USER/PATIENT
Device Availability*
Device AgeNA
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerALIMED INC
Manufacturer Address297 HIGH STREET DEDHAM MA 02026 US 02026


Patients

Patient NumberTreatmentOutcomeDate
001. Death 2018-06-20

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