ACROBAT-I STABILIZER Adverse Event — Malfunction (MDR 10000395)
ACROBAT-I STABILIZER Adverse Event — Malfunction (MDR 10000395) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ACROBAT-I STABILIZER; Generic name: STABILIZER,HEART; Manufacturer: MAQUET CARDIOVASCULAR LLC.
| Device | ACROBAT-I STABILIZER |
|---|---|
| Generic name | STABILIZER,HEART |
| Manufacturer | MAQUET CARDIOVASCULAR LLC |
| Report number | 10000395 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | AT THE END OF OPERATING ROOM CASE, PLASTIC LOCK TO THE MAQUET RETRACTOR WAS MISSING. IT IS NOT RADIOPAQUE. |
| Source | openFDA MAUDE (device adverse events) |
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