AED PLUS Adverse Event — Malfunction (MDR 1220908-2008-00283)
AED PLUS Adverse Event — Malfunction (MDR 1220908-2008-00283) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AED PLUS; Generic name: DEFIBRILLATOR; Manufacturer: ZOLL MEDICAL CORPORATION.
| Device | AED PLUS |
|---|---|
| Generic name | DEFIBRILLATOR |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Report number | 1220908-2008-00283 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | User facility |
| Narrative | COMPLAINANT ALLEGED THAT WHILE ATTEMPTING TO MONITOR A PT, THE DEVICE INAPPROPRIATELY SHUT DOWN. COMPLAINANT INDICATED THAT THE CLINICIAN OBTAINED ANOTHER DEVICE TO CONTINUE TREATING THE PT. COMPLAINANT INDICATED THAT THERE WAS NO ADVERSE EFFECT TO THE PT DUE TO THE REPORTED MALFUNCTION. |
| Source | openFDA MAUDE (device adverse events) |
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