ZOLL Adverse Event — Injury (MDR MW5005564)
ZOLL Adverse Event — Injury (MDR MW5005564) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ZOLL; Generic name: R-SERIES DEFIBRILLATOR; Manufacturer: ZOLL MEDICAL CORPORATION.
| Device | ZOLL |
|---|---|
| Generic name | R-SERIES DEFIBRILLATOR |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Report number | MW5005564 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-18 |
| Narrative | MALE PT WITH CHEST PAIN. CHEST SHAVED/CLIPPED AND ZOLL RADIOLUCENT PRO-PADZ II ELECTRODES (ITEM # 8900-4005) APPLIED. PT TO CARDIAC CATH LAB. IN CATH LAB, ELECTRODES CONNECTED TO ZOLL R SERIES DEFIBRILLATOR. PT WENT INTO V-FIB, UNABLE TO DEFIBRILLATE PATIENT. MANUAL PRESSURE APPLIED TO ELECTRODES. SECOND ATTEMPT TO DEFIBRILLATE SUCCESSFUL. PT RESUSCITATED. NO LONG TERM HARM TO PATIENT. TWO SIMILAR |
| Source | openFDA MAUDE (device adverse events) |
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