HEARTSTART FRX Adverse Event — Malfunction (MDR 3030677-2020-00708)
HEARTSTART FRX Adverse Event — Malfunction (MDR 3030677-2020-00708) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: HEARTSTART FRX; Generic name: AED; Manufacturer: PHILIPS MEDICAL SYSTEMS.
| Device | HEARTSTART FRX |
|---|---|
| Generic name | AED |
| Manufacturer | PHILIPS MEDICAL SYSTEMS |
| Report number | 3030677-2020-00708 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | THIS DEVICE WAS RETURNED WITHOUT AN ALLEGATION FROM THE CUSTOMER, BUT AN ISSUE WAS FOUND IN THE DATA LOGS. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →