ZYNEX NEXWAVE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 99 report with the FDA on 2015-03-13 for ZYNEX NEXWAVE manufactured by Zynex Medical, Inc..

Event Text Entries

[5659873] Received unit with letter from law firm claiming patient injury, but no specific as to type of injury reported.
Patient Sequence No: 1, Text Type: D, B5


[13032055] Zynex: unit returned through front door, but not as a qa return. Low firm letter enclosed. No specifics on problem other than "personal injury" unit was tested and functioned according to spec. No problem found. Law letter could be from a billing perspective and not necessary the unit.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1723686-2015-00013
MDR Report Key4613383
Report Source99
Date Received2015-03-13
Date of Report2015-03-11
Date of Event2014-06-21
Date Mfgr Received2014-06-21
Device Manufacturer Date2012-06-01
Date Added to Maude2015-04-27
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 Street9990 PARK MEADOWS DRIVE
Manufacturer CityLONE TREE CO 80124
Manufacturer CountryUS
Manufacturer Postal80124
Manufacturer Phone3037034906
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameZYNEX
Generic NameELECTRICAL STIMULATOR
Product CodeIPF
Date Received2015-03-13
Returned To Mfg2014-06-21
Model NumberNEXWAVE
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZYNEX MEDICAL, INC.


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-03-13

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