MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2014-03-25 for OXIMAX N-560 PULSE OXIMETER N560 manufactured by Mediana.
[21444686]
It was reported to covidien that the oximax n560 pulse oximeter display was missing segments. There was no pt involvement.
Patient Sequence No: 1, Text Type: D, B5
[21664090]
Covidien verified that the display was missing segments. The problem was isolated to the front pcb. The root cause was determined to be cold/cracked solder joints. (b)(4). Serial number of the front pcb precedes a corrective and preventive action taken by the manufacturer.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2936999-2014-00283 |
| MDR Report Key | 3815794 |
| Report Source | 06 |
| Date Received | 2014-03-25 |
| Date of Report | 2014-03-19 |
| Date of Event | 2014-03-18 |
| Date Mfgr Received | 2014-03-19 |
| Device Manufacturer Date | 2012-11-01 |
| Date Added to Maude | 2014-06-13 |
| 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 Contact | DENISE BRAXTON |
| Manufacturer Street | 6135 GUNBARREL AVE |
| Manufacturer City | BOULDER CO 80301 |
| Manufacturer Country | US |
| Manufacturer Postal | 80301 |
| Manufacturer Phone | 3038768909 |
| Manufacturer G1 | MEDIANA |
| Manufacturer Street | WONJU INDUSTRY PARK DONGWHA-RI, MUNMAK-EUP, WONJU-SI |
| Manufacturer City | GANGWON-DO |
| Manufacturer Country | KS |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | OXIMAX N-560 PULSE OXIMETER |
| Generic Name | PULSE OXIMETER |
| Product Code | DPZ |
| Date Received | 2014-03-25 |
| Returned To Mfg | 2014-03-24 |
| Model Number | N-560 |
| Catalog Number | N560 |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDIANA |
| Manufacturer Address | WONJU INDUSTRY PARK DONGWHA-RI, MUNMAK-EUP GANGWON KS |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2014-03-25 |