UNKNOWN LINER Adverse Event — Injury (MDR 0001822565-2020-01552)
UNKNOWN LINER Adverse Event — Injury (MDR 0001822565-2020-01552) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN LINER; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER BIOMET, INC..
| Device | UNKNOWN LINER |
|---|---|
| Generic name | PROSTHESIS, HIP |
| Manufacturer | ZIMMER BIOMET, INC. |
| Report number | 0001822565-2020-01552 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | DISTRIBUTOR, HEALTH PROFESSION |
| Narrative | THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. REPORTED EVENT WAS CONFIRMED. RADIOGRAPHS WERE PROVIDED AND REVIEWED BY A HEALTH CARE PROFESSIONAL. REVIEW OF THE AVAILABLE RECORDS IDENTIFIED THE FOLLOWING: MARKED ECCENTRIC POSITION OF THE LEFT FEMORAL HEAD REFLECTING ADVANCED LINER WEAR AS NOTED. NO FURTHER EVALUATION COULD BE PERFORMED. DEVICE HISTORY RECORD (DHR) WAS RE |
| Source | openFDA MAUDE (device adverse events) |
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