MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-09-22 for LIONVILLE LOCK ALERT II 800 SERIES * manufactured by Intermetro Industries Corp..
[14965427]
The batteries are not able to charge due to power supply failure which causes the cart not to function. Patient care is adversely affected because medication can not be distributed to patients in a timely manner due to maintenance constantly being performed on medication carts. ====================== manufacturer response for medication cart, lock alert ii======================the manufacturer sent a replacement power supply and wiring harness.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1846329 |
| MDR Report Key | 1846329 |
| Date Received | 2010-09-22 |
| Date of Report | 2010-08-04 |
| Date of Event | 2010-08-04 |
| Report Date | 2010-08-04 |
| Date Reported to FDA | 2010-09-22 |
| Date Added to Maude | 2010-09-28 |
| 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 LOCK ALERT II |
| Generic Name | MEDICATION CART |
| Product Code | NXB |
| Date Received | 2010-09-22 |
| Model Number | 800 SERIES |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | NURSE |
| Device Availability | Y |
| Device Age | 2 YR |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | INTERMETRO INDUSTRIES CORP. |
| Manufacturer Address | 651 NORTH WASHINGTON ST. WILKES BARRE PA 18705 US 18705 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2010-09-22 |