BIGLIANI/FLATOW COMPLETE SHOULDER Adverse Event — Injury (MDR 3005751028-2008-00002)
BIGLIANI/FLATOW COMPLETE SHOULDER Adverse Event — Injury (MDR 3005751028-2008-00002) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BIGLIANI/FLATOW COMPLETE SHOULDER; Generic name: GLENOID COMPONENT; Manufacturer: ZIMMER TMT.
| Device | BIGLIANI/FLATOW COMPLETE SHOULDER |
|---|---|
| Generic name | GLENOID COMPONENT |
| Manufacturer | ZIMMER TMT |
| Report number | 3005751028-2008-00002 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional |
| Narrative | THE PATIENT SUFFERED A TRAUMATIC EVENT, WHEN HE ATTEMPTED TO CATCH A FALLING TABLE, WHICH WEIGHED GREATER THAN 200 LBS. RADIOGRAPHIC EVALUATION OF THE PATIENT SUBSEQUENT TO THE EVENT REVEALED THAT THE IMPLANT HAD FRACTURED. THE PATIENT WAS SUCCESSFULLY REVISED. |
| Source | openFDA MAUDE (device adverse events) |
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