LD304 MATERNITY BED Adverse Event — Malfunction (MDR 0001831750-2020-00476)
LD304 MATERNITY BED Adverse Event — Malfunction (MDR 0001831750-2020-00476) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LD304 MATERNITY BED; Generic name: TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES); Manufacturer: STRYKER MEDICAL-KALAMAZOO.
| Device | LD304 MATERNITY BED |
|---|---|
| Generic name | TABLE, OBSTETRICAL, AC-POWERED (AND ACCESSORIES) |
| Manufacturer | STRYKER MEDICAL-KALAMAZOO |
| Report number | 0001831750-2020-00476 |
| 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. THE DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; 1 DEVICE HAD A LOOSE COMPONENT, 1 DEVICE HAD A MISSING COMPONENT, 1 DEVICE HAD A BROKEN/DAMAGED COMPONENT, AND 1 DEVICE HAD A DETACHED COMPONENT. THE DEVICES WERE REPAIRED AND RETURNED. THERE WAS NO REMEDIAL ACTIO |
| Source | openFDA MAUDE (device adverse events) |
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