VERSACARE FRAME Adverse Event — Malfunction (MDR 1824206-2020-00190)
VERSACARE FRAME Adverse Event — Malfunction (MDR 1824206-2020-00190) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VERSACARE FRAME; Generic name: BED, AC-POWERED ADJUSTABLE HOSPITAL; Manufacturer: HILL-ROM BATESVILLE.
| Device | VERSACARE FRAME |
|---|---|
| Generic name | BED, AC-POWERED ADJUSTABLE HOSPITAL |
| Manufacturer | HILL-ROM BATESVILLE |
| Report number | 1824206-2020-00190 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, USER F |
| Narrative | THE HILLROM TECHNICIAN FOUND THE BRAKE CASTERS NEEDED TO BE REPLACED. PER THE HILLROM SERVICE MANUAL, PERFORM ANNUAL PREVENTIVE MAINTENANCE PROCEDURES TO MAKE SURE ALL VERSACARE® BED COMPONENTS ARE FUNCTIONING AS ORIGINALLY DESIGNED. BRAKE CASTERS SHOULD BE CHECKED FOR CUTS, WEAR AND QUALITY OF TREAD, ETC. AND REPLACED WHEN NECESSARY. EXAMINE THE BRAKES TO SEE WHETHER THE BED MOVES WHEN THE BRAKE |
| Source | openFDA MAUDE (device adverse events) |
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