UNKNOWN ANCHORAGE LAPIDUS STEP 0MM RIGHT PLATE Adverse Event — Injury (MDR 0008031020-2020-01403)
UNKNOWN ANCHORAGE LAPIDUS STEP 0MM RIGHT PLATE Adverse Event — Injury (MDR 0008031020-2020-01403) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN ANCHORAGE LAPIDUS STEP 0MM RIGHT PLATE; Generic name: IMPLANT; Manufacturer: STRYKER GMBH.
| Device | UNKNOWN ANCHORAGE LAPIDUS STEP 0MM RIGHT PLATE |
|---|---|
| Generic name | IMPLANT |
| Manufacturer | STRYKER GMBH |
| Report number | 0008031020-2020-01403 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | STUDY |
| Narrative | THE REPORTED EVENT COULD NOT BE CONFIRMED, SINCE THE DEVICE WAS NOT RETURNED FOR EVALUATION AND NO OTHER ADDITIONAL INFORMATION IS AVAILABLE. MORE DETAILED INFORMATION ABOUT THE COMPLAINT EVENT AS WELL AS THE AFFECTED DEVICE MUST BE AVAILABLE IN ORDER TO DETERMINE THE ROOT CAUSE OF THE COMPLAINT EVENT. THE DEVICE HISTORY RECORD COULD NOT BE REVIEWED BECAUSE THE AFFECTED LOT NUMBER WAS NOT COMMUNIC |
| Source | openFDA MAUDE (device adverse events) |
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