INDURA Adverse Event — Injury (MDR 6000030-2008-00803)
INDURA Adverse Event — Injury (MDR 6000030-2008-00803) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INDURA; Manufacturer: RICE CREEK MANUFACTURING; Report number: 6000030-2008-00803.
| Device | INDURA |
|---|---|
| Manufacturer | RICE CREEK MANUFACTURING |
| Report number | 6000030-2008-00803 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2008-02-19 |
| Report source | Consumer |
| Narrative | THE PATIENT REPORTED THAT SHE WAS REACHING FOR A FALLING CABINET AND IT RESULTED IN HER CATHETER BEING BROKEN. NO PATIENT SYMPTOMS WERE REPORTED. THE TYPE OF MEDICATION, CONCENTRATION, AND DAILY DOSE BEING ADMINISTERED VIA THE PUMP WERE NOT REPORTED; DEVICE REGISTRATION SYSTEM INDICATES MORPHINE. ADDITIONAL INFORMATION HAS BEEN REQUESTED, A FOLLOW-UP REPORT WILL BE SENT IF ADDITIONAL INFORMATION B |
| Source | openFDA MAUDE (device adverse events) |
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