ZOLL Adverse Event — Injury (MDR MW5005565)
ZOLL Adverse Event — Injury (MDR MW5005565) 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 | MW5005565 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-18 |
| Narrative | ZOLL R-SERIES DEFIBRILLATOR + ZOLL "ONE STEP CPRA/A RESUSCITATION ELECTRODE (ITEM) CONNECTED TO PT. UNABLE TO DEFIBRILLATE PT ELECTRODES CHANGED ABLE TO DEFIBRILLATE PT. IT APPEARS THE ELECTRODE PACKAGE WAS OPENED INCORRECTLY, LEAVING "SELF TEST JUMPER" INTACT, CAUSING "DEFIB PAD SHORT" MESSAGE & INABILITY TO DEFIBRILLATE PT. PROBLEM DISCUSSED WITH MANUFACTURER 1/3/08. FOR MORE DETAILS, CONTACT ME |
| Source | openFDA MAUDE (device adverse events) |
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