TRURIZE Adverse Event — Injury (MDR 0001831750-2020-00546)
TRURIZE Adverse Event — Injury (MDR 0001831750-2020-00546) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRURIZE; Generic name: CHAIR, POSITIONING, ELECTRIC; Manufacturer: STRYKER MEDICAL-KALAMAZOO.
| Device | TRURIZE |
|---|---|
| Generic name | CHAIR, POSITIONING, ELECTRIC |
| Manufacturer | STRYKER MEDICAL-KALAMAZOO |
| Report number | 0001831750-2020-00546 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | UPON INSPECTION OF THE TRURIZE CHAIR AFTER THE EVENT BY THE USER FACILITY, THE CORD THAT ATTACHED IT TO THE STAFF CALL SYSTEM WAS FOUND TO HAVE A BENT PRONG. THE BENT PRONG DID NOT ALLOW THE CHAIR EXIT ALARM TO BE CONNECTED TO THE CALL SYSTEM. |
| Source | openFDA MAUDE (device adverse events) |
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