MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-01-10 for COLOR DOPPLER ULTRASOUND HP77021A manufactured by Hewlett Packard Co..
[7513]
Ultrasound picks up rf noise from another co's pacer/monitor. (also see medwatch 1000382 and 1000383. )
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1000381 |
| MDR Report Key | 10930 |
| Date Received | 1994-01-10 |
| Date Added to Maude | 1994-01-13 |
| 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 |
| Reporter Occupation | BIOMEDICAL ENGINEER |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | COLOR DOPPLER ULTRASOUND |
| Product Code | DXK |
| Date Received | 1994-01-10 |
| Model Number | HP77021A |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 10930 |
| Manufacturer | HEWLETT PACKARD CO. |
| Manufacturer Address | ANDOVER MA 01810 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1994-01-10 |