ARTHRO RASP 20 DOWNBEND *EA Adverse Event — Malfunction (MDR 1221934-2020-01259)
ARTHRO RASP 20 DOWNBEND *EA Adverse Event — Malfunction (MDR 1221934-2020-01259) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ARTHRO RASP 20 DOWNBEND *EA; Generic name: BONE RASP; Manufacturer: DEPUY MITEK LLC US.
| Device | ARTHRO RASP 20 DOWNBEND *EA |
|---|---|
| Generic name | BONE RASP |
| Manufacturer | DEPUY MITEK LLC US |
| Report number | 1221934-2020-01259 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN |
| Narrative | PRODUCT COMPLAINT #: (B)(4). DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. UDI: (B)(4). THE LOT NUMBER IS UNKNOWN. |
| Source | openFDA MAUDE (device adverse events) |
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