TPRLC 133 MP TYPE1 PPS SO 16.0 1 Adverse Event — Malfunction (MDR 0001825034-2020-01723)
TPRLC 133 MP TYPE1 PPS SO 16.0 1 Adverse Event — Malfunction (MDR 0001825034-2020-01723) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TPRLC 133 MP TYPE1 PPS SO 16.0 1; Generic name: PROSTHEISI, HIP; Manufacturer: ZIMMER BIOMET, INC..
| Device | TPRLC 133 MP TYPE1 PPS SO 16.0 1 |
|---|---|
| Generic name | PROSTHEISI, HIP |
| Manufacturer | ZIMMER BIOMET, INC. |
| Report number | 0001825034-2020-01723 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | UPON INVESTIGATION, IT HAS BEEN DETERMINED THAT THE DEBRIS IN THE STERILE PACKAGING DID NOT COMPROMISE STERILITY. EVENT IS NO LONGER CONSIDERED REPORTABLE, AND INITIAL REPORT SHOULD BE VOIDED. |
| Source | openFDA MAUDE (device adverse events) |
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