VERSACARE FRAME Adverse Event — Malfunction (MDR 1824206-2020-00192)
VERSACARE FRAME Adverse Event — Malfunction (MDR 1824206-2020-00192) 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 | 1824206-2020-00192 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, USER F |
| Narrative | THE HILLROM TECHNICIAN FOUND THE EXTERNAL ALARM NEEDED TO BE REPLACED. THE EXTERNAL ALARM IS THE SOURCE OF THE BRAKE NOT SET ALARM. PER THE HILLROM SERVICE MANUAL, PERFORM ANNUAL PREVENTIVE MAINTENANCE PROCEDURES TO MAKE SURE ALL VERSACARE® BED COMPONENTS ARE FUNCTIONING AS ORIGINALLY DESIGNED. MAKE SURE THE BRAKE IS NOT SET, AND THEN PLUG THE BED INTO AN APPLICABLE POWER SOURCE. A STEADY ALARM CO |
| Source | openFDA MAUDE (device adverse events) |
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