MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-10-05 for LIONVILLE 800 * manufactured by Intermetro Industries Corp..
[1770061]
Medication cart power supply battery harness connectors overheat and fail. ====================== manufacturer response for medication cart with computer and ups, lionville======================problem has occurred on several medication carts. The manufacturer replaced batteries and power supplies on several.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1863409 |
MDR Report Key | 1863409 |
Date Received | 2010-10-05 |
Date of Report | 2010-09-30 |
Date of Event | 2010-09-27 |
Report Date | 2010-09-30 |
Date Reported to FDA | 2010-10-05 |
Date Added to Maude | 2010-10-10 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LIONVILLE |
Generic Name | MEDICATION CART WITH COMPUTER AND UPS |
Product Code | NXB |
Date Received | 2010-10-05 |
Model Number | 800 |
Catalog Number | * |
Lot Number | * |
ID Number | * |
Device Availability | Y |
Device Age | 2 YR |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INTERMETRO INDUSTRIES CORP. |
Manufacturer Address | 1101 N. WASHINGTON ST. WILKES-BARRE PA 18705 US 18705 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2010-10-05 |