ZYNEX

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2015-02-11 for ZYNEX manufactured by Zynex Medical Inc.

Event Text Entries

[5559093] Patient reported receiving excess stimulation when unit is powered on. Unit increases excessively in stim on it's own.
Patient Sequence No: 1, Text Type: D, B5


[12952717] Reporting due to fda findings during audit in 01/2015. Investigation and results: unit turned on, passed final testing without any problems. Left unit running for 25 minutes at 23ma (tens mode) and had no excessive increase on it's own. Could not duplicate patients complaint. No problem found.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1723686-2015-00003
MDR Report Key4574818
Report Source04
Date Received2015-02-11
Date of Report2015-02-05
Date of Event2014-03-17
Date Mfgr Received2014-03-17
Device Manufacturer Date2014-02-24
Date Added to Maude2015-03-17
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 DR
Manufacturer CityLONE TREE CO 80124
Manufacturer CountryUS
Manufacturer Postal80124
Manufacturer Phone8004956670
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameZYNEX
Generic NameNEXWAVE
Product CodeIPF
Date Received2015-02-11
Returned To Mfg2014-03-28
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZYNEX MEDICAL INC
Manufacturer AddressLONE TREE CO 80124 US 80124


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-02-11

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