ROTICULATOR ENDO GRASP 5MM W/SPIN LOCK Adverse Event — Malfunction (MDR 2647580-2008-00077)
ROTICULATOR ENDO GRASP 5MM W/SPIN LOCK Adverse Event — Malfunction (MDR 2647580-2008-00077) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ROTICULATOR ENDO GRASP 5MM W/SPIN LOCK; Generic name: ROTICULATOR ENDO GRASP; Manufacturer: PONCE - USS.
| Device | ROTICULATOR ENDO GRASP 5MM W/SPIN LOCK |
|---|---|
| Generic name | ROTICULATOR ENDO GRASP |
| Manufacturer | PONCE - USS |
| Report number | 2647580-2008-00077 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-19 |
| Report source | Health Professional |
| Narrative | ACCORDING TO THE REPORTER: WHEN THE GRASPER WAS STRAIGHTENED IT BROKE. NO REPORT OF IMPACT TO PT AND PT INJURY. ANOTHER DEVICE WAS USED. PROCEDURE: LAP NISSEN. |
| Source | openFDA MAUDE (device adverse events) |
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