GOBED II MED/SURG BED Adverse Event — Malfunction (MDR 0001831750-2020-00613)
GOBED II MED/SURG BED Adverse Event — Malfunction (MDR 0001831750-2020-00613) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: GOBED II MED/SURG BED; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: STRYKER MEDICAL-KALAMAZOO.
| Device | GOBED II MED/SURG BED |
|---|---|
| Generic name | BED, AC-POWERED ADJUSTABLE HOSPITAL |
| Manufacturer | STRYKER MEDICAL-KALAMAZOO |
| Report number | 0001831750-2020-00613 |
| 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 DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; THERE WERE BROKEN/DAMAGED COMPONENTS. THE DEVICES WERE REPAIRED AND RETURNED. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FOR SINGLE USE. |
| Source | openFDA MAUDE (device adverse events) |
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