UNKNOWN_SIMPLEX P SPEEDSET BONE CEMENT Adverse Event — Injury (MDR 0002249697-2020-00810)
UNKNOWN_SIMPLEX P SPEEDSET BONE CEMENT Adverse Event — Injury (MDR 0002249697-2020-00810) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN_SIMPLEX P SPEEDSET BONE CEMENT; Generic name: BONE CEMENT; Manufacturer: STRYKER ORTHOPAEDICS-MAHWAH.
| Device | UNKNOWN_SIMPLEX P SPEEDSET BONE CEMENT |
|---|---|
| Generic name | BONE CEMENT |
| Manufacturer | STRYKER ORTHOPAEDICS-MAHWAH |
| Report number | 0002249697-2020-00810 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| Report source | CONSUMER, OTHER |
| Narrative | THE INFORMATION IN THIS REPORT WAS PROVIDED BY STRYKER ORTHOPAEDICS LEGAL AFFAIRS DEPARTMENT. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME DUE TO THE ONGOING LITIGATION. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, THE EVALUATION SUMMARY WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →