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..
[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
Report Number | 1723686-2015-00013 |
MDR Report Key | 4613383 |
Report Source | 99 |
Date Received | 2015-03-13 |
Date of Report | 2015-03-11 |
Date of Event | 2014-06-21 |
Date Mfgr Received | 2014-06-21 |
Device Manufacturer Date | 2012-06-01 |
Date Added to Maude | 2015-04-27 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Street | 9990 PARK MEADOWS DRIVE |
Manufacturer City | LONE TREE CO 80124 |
Manufacturer Country | US |
Manufacturer Postal | 80124 |
Manufacturer Phone | 3037034906 |
Single Use | 3 |
Remedial Action | RL |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ZYNEX |
Generic Name | ELECTRICAL STIMULATOR |
Product Code | IPF |
Date Received | 2015-03-13 |
Returned To Mfg | 2014-06-21 |
Model Number | NEXWAVE |
Operator | LAY USER/PATIENT |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ZYNEX MEDICAL, INC. |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2015-03-13 |