GOBED II Adverse Event — Malfunction (MDR 0001831750-2020-00319)
GOBED II Adverse Event — Malfunction (MDR 0001831750-2020-00319) 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 | 0001831750-2020-00319 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | THIS MDR IS PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. 1 DEVICES WERE EVALUATED IN THE FIELD BUT THE ISSUE WAS NOT CONFIRMED; NO DEFECT OR MALFUNCTION WAS FOUND. 3 DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; 1 DEVICE HAD A BROKEN/DAMAGED COMPONENT, 1 DEVICE HAD CORROSION, AND 1 DEVICE HAD ALIGNMENT ISSUES. THE DEVICES WERE REPAIRED AND RETURNED. 1 DEVICE |
| Source | openFDA MAUDE (device adverse events) |
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