G3 PLUS AUTO, AED, AHA 2010, US ENGLISH Adverse Event — Malfunction (MDR 2112020-2020-00320)
G3 PLUS AUTO, AED, AHA 2010, US ENGLISH Adverse Event — Malfunction (MDR 2112020-2020-00320) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: G3 PLUS AUTO, AED, AHA 2010, US ENGLISH; Generic name: AUTOMATED EXTERNAL DEFIBRILLATOR; Manufacturer: CARDIAC SCIENCE CORPORATION.
| Device | G3 PLUS AUTO, AED, AHA 2010, US ENGLISH |
|---|---|
| Generic name | AUTOMATED EXTERNAL DEFIBRILLATOR |
| Manufacturer | CARDIAC SCIENCE CORPORATION |
| Report number | 2112020-2020-00320 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | ZOLL MEDICAL CORPORATION HAS NOT RECEIVED THE DEVICE FOR EVALUATION AND THIS COMPLAINT IS STILL UNDER INVESTIGATION. |
| Source | openFDA MAUDE (device adverse events) |
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