MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2013-02-06 for ADVANTX-E LC+ manufactured by Ge Medical Systems Scs.
[3141329]
It was reported that images on the exam room live monitor were flickering. The user stated that when the monitor was flickering the images were unusable. This issue may result in a degraded image quality that can prevent completion of an exam. No patient injury or death reported.
Patient Sequence No: 1, Text Type: D, B5
[10514377]
Ge healthcare? S investigation is ongoing. A follow up report will be submitted once the investigation has been completed. This malfunction was determined to be reportable as this same malfunction has previously contributed to a serious injury within the last two years. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
Report Number | 9611343-2013-00001 |
MDR Report Key | 2958200 |
Report Source | 01,05,06 |
Date Received | 2013-02-06 |
Date of Report | 2013-01-08 |
Date of Event | 2013-01-08 |
Date Mfgr Received | 2013-01-08 |
Device Manufacturer Date | 1999-02-01 |
Date Added to Maude | 2013-04-19 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | JOY SONSALLA |
Manufacturer Street | 3000 N. GRANDVIEW BLVD. |
Manufacturer City | WAUKESHA WI 53188 |
Manufacturer Country | US |
Manufacturer Postal | 53188 |
Manufacturer Phone | 2625482661 |
Manufacturer G1 | GE MEDICAL SYSTEMS SCS |
Manufacturer Street | 283 RUE DE LA MINIERE BP 34 |
Manufacturer City | BUC CEDEX |
Manufacturer Country | FR |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ADVANTX-E LC+ |
Generic Name | ANGIOGRAPHIC X-RAY SYSTEM |
Product Code | IZO |
Date Received | 2013-02-06 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GE MEDICAL SYSTEMS SCS |
Manufacturer Address | 283 RUE DE LA MINIERE BP 34 BUC CEDEX FR |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2013-02-06 |