SPIRIT SELECT Adverse Event — Malfunction (MDR 3006433555-2020-00017)
SPIRIT SELECT Adverse Event — Malfunction (MDR 3006433555-2020-00017) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SPIRIT SELECT; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: STRYKER MEDICAL LONDON DBA CHG HOSPITAL BEDS.
| Device | SPIRIT SELECT |
|---|---|
| Generic name | BED, AC-POWERED ADJUSTABLE HOSPITAL |
| Manufacturer | STRYKER MEDICAL LONDON DBA CHG HOSPITAL BEDS |
| Report number | 3006433555-2020-00017 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | THIS MDR IS PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. THE DEVICE WAS EVALUATED IN THE FIELD BUT THE ISSUE WAS NOT CONFIRMED; NO DEFECT OR MALFUNCTION WAS FOUND. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FOR SINGLE USE. |
| Source | openFDA MAUDE (device adverse events) |
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