GOBED II Adverse Event — Malfunction (MDR 0001831750-2020-00548)
GOBED II Adverse Event — Malfunction (MDR 0001831750-2020-00548) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: GOBED II; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: STRYKER MEDICAL-KALAMAZOO.
| Device | GOBED II |
|---|---|
| Generic name | BED, AC-POWERED ADJUSTABLE HOSPITAL |
| Manufacturer | STRYKER MEDICAL-KALAMAZOO |
| Report number | 0001831750-2020-00548 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| 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. 4 DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; THE DEVICES HAD BROKEN/DAMAGED COMPONENTS. THE DEVICES WERE REPA |
| Source | openFDA MAUDE (device adverse events) |
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