SPIRIT SELECT Adverse Event — Malfunction (MDR 3006433555-2020-00012)
SPIRIT SELECT Adverse Event — Malfunction (MDR 3006433555-2020-00012) 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 | 3006433555-2020-00012 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | THIS MDR IS A CONSOLIDATION OF RECORDS SUMMARIZED AS PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. 1 DEVICE WAS NOT EVALUATED, AS THE ISSUE WAS IDENTIFIED AND RESOLVED DURING A TROUBLESHOOTING CALL BETWEEN THE CUSTOMER AND STRYKER TECHNICAL SUPPORT. 25 DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; 3 DEVICES HAD BENT COMPONENTS, 2 DEVICES HAD STRIPPED COMPONENT |
| Source | openFDA MAUDE (device adverse events) |
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