S3 PX1-3005 Adverse Event — Malfunction (MDR 0001831750-2020-00377)
S3 PX1-3005 Adverse Event — Malfunction (MDR 0001831750-2020-00377) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: S3 PX1-3005; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: STRYKER MEDICAL-KALAMAZOO.
| Device | S3 PX1-3005 |
|---|---|
| Generic name | BED, AC-POWERED ADJUSTABLE HOSPITAL |
| Manufacturer | STRYKER MEDICAL-KALAMAZOO |
| Report number | 0001831750-2020-00377 |
| 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 EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; THE DEVICE HAD A BROKEN/DAMAGED COMPONENT. THE DEVICES WERE REPAIRED AND RETURNED. 1 DEVICE WAS EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED. HOWEVER, THERE WAS NO PRODUCT MALFUNCTION; THE ISSUE WAS THE RESULT O |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →