STAIR PRO - MODEL 6252 Adverse Event — Malfunction (MDR 0001831750-2020-00569)
STAIR PRO - MODEL 6252 Adverse Event — Malfunction (MDR 0001831750-2020-00569) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: STAIR PRO - MODEL 6252; Generic name: STRETCHER, HAND-CARRIED; Manufacturer: STRYKER MEDICAL-KALAMAZOO.
| Device | STAIR PRO - MODEL 6252 |
|---|---|
| Generic name | STRETCHER, HAND-CARRIED |
| Manufacturer | STRYKER MEDICAL-KALAMAZOO |
| Report number | 0001831750-2020-00569 |
| 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. 5 DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; 4 DEVICES HAD MISSING COMPONENTS AND 1 DEVICE HAD A BROKEN/DAMAGED COMPONENT. THE DEVICES WERE REPAIRED AND RETURNED. 1 DEVICE IS PENDING EVALUATION. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FO |
| Source | openFDA MAUDE (device adverse events) |
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