GOBED II Adverse Event — Malfunction (MDR 0001831750-2020-00365)
GOBED II Adverse Event — Malfunction (MDR 0001831750-2020-00365) 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 | 0001831750-2020-00365 |
| 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 AND THE ISSUE WAS NOT CONFIRMED, AS THE CUSTOMER DID NOT MAKE THE DEVICE AVAILABLE FOR EVALUATION. 1 DEVICE WAS EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; THE DEVICE HAD AN INCORRECT/INCOMPATIBLE COMPONENT. THE DEVICES WERE REPAIRED AND RETURNED. |
| Source | openFDA MAUDE (device adverse events) |
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