COMMUNICATOR 6290

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2018-10-29 for COMMUNICATOR 6290 manufactured by External Manufacturer.

Event Text Entries

[125341864] The product is expected to be returned for analysis. This report will be updated upon return and completion of analysis.
Patient Sequence No: 1, Text Type: N, H10


[125341865] Boston scientific received information that the communicator? S electricity cable was melted. A boston scientific company representative verified that there was a recent storm. The company representative also noted that the patient's date of birth (dob) was incorrect in the system. The physician sent a cable to the patient and will revert back to patient services if the issue persisted. The communicator remains in service. No adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2124215-2018-14754
MDR Report Key8015500
Report SourceCONSUMER
Date Received2018-10-29
Date of Report2018-07-25
Date of Event2018-07-24
Date Mfgr Received2018-07-25
Date Added to Maude2018-10-29
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 ContactTIM DEGROOT
Manufacturer Street4100 HAMLINE AVE. N
Manufacturer CityST. PAUL MN
Manufacturer Phone6515826168
Manufacturer G1EXTERNAL MANUFACTURER
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOMMUNICATOR
Generic NameACCESSORY
Product CodeOSR
Date Received2018-10-29
Model Number6290
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEXTERNAL MANUFACTURER


Patients

Patient NumberTreatmentOutcomeDate
10 2018-10-29

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