SROM TRI BAND CONE REAMER 19 Adverse Event — Malfunction (MDR 1818910-2020-11320)
SROM TRI BAND CONE REAMER 19 Adverse Event — Malfunction (MDR 1818910-2020-11320) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SROM TRI BAND CONE REAMER 19; Generic name: HIP INSTRUMENTS : REAMERS; Manufacturer: DEPUY ORTHOPAEDICS INC US.
| Device | SROM TRI BAND CONE REAMER 19 |
|---|---|
| Generic name | HIP INSTRUMENTS : REAMERS |
| Manufacturer | DEPUY ORTHOPAEDICS INC US |
| Report number | 1818910-2020-11320 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | PRODUCT COMPLAINT #: (B)(4). IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. |
| Source | openFDA MAUDE (device adverse events) |
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