MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-07-25 for HI-PINNACLE manufactured by Howard Medical.
[18792329]
Notified that a hi-pinnacle medication cart from (b)(6) had caught fire after the morning medication pass. The nurse had completed her medication pass and plugged the cart back in to charge when noticed sparking and smoke coming from cart. Removed cart to outside area and used fire extinguisher to extinguish cart.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5037471 |
| MDR Report Key | 3966357 |
| Date Received | 2014-07-25 |
| Date of Report | 2014-07-24 |
| Date of Event | 2014-07-21 |
| Date Added to Maude | 2014-07-30 |
| Event Key | 0 |
| Report Source Code | Voluntary 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 | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HI-PINNACLE |
| Generic Name | MEDICATION CART |
| Product Code | BRY |
| Date Received | 2014-07-25 |
| Operator | HEALTH PROFESSIONAL |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | HOWARD MEDICAL |
| Manufacturer Address | ELLISVILLE 39437 39437 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2014-07-25 |