STARDRIVE SCREWDRIVER SHAFT T8 SELF-RETAINING/QC Adverse Event — Malfunction (MDR 8030965-2020-03121)
STARDRIVE SCREWDRIVER SHAFT T8 SELF-RETAINING/QC Adverse Event — Malfunction (MDR 8030965-2020-03121) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: STARDRIVE SCREWDRIVER SHAFT T8 SELF-RETAINING/QC; Generic name: APPLIANCE,FIXATION,SPINAL INTERVERTEBRAL BODY; Manufacturer: OBER
| Device | STARDRIVE SCREWDRIVER SHAFT T8 SELF-RETAINING/QC |
|---|---|
| Generic name | APPLIANCE,FIXATION,SPINAL INTERVERTEBRAL BODY |
| Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
| Report number | 8030965-2020-03121 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | COMPLAINANT PART IS EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION, BUT HAS YET TO BE RECEIVED. THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS NO PRODUCT WAS RECEIVED. BASED ON THE INFORMATION AVAILABLE, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. THIS COMPLAINT WILL BE ACCOUNTED FOR AND MONITORED VIA POST MARKET SURV |
| Source | openFDA MAUDE (device adverse events) |
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