MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2016-04-20 for ACORN STAIRLIFT 180 manufactured by Acorn Mobility Services Ltd.
[43174030]
Customer called that whilst dismounting stairlift at bottom of stairway seatbase snapped off.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3006310491-2016-00002 |
| MDR Report Key | 5590004 |
| Report Source | CONSUMER |
| Date Received | 2016-04-20 |
| Date of Report | 2016-03-18 |
| Date of Event | 2016-02-27 |
| Date Mfgr Received | 2016-02-27 |
| Device Manufacturer Date | 2013-03-01 |
| Date Added to Maude | 2016-04-20 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR WILLIAM WADDELL |
| Manufacturer Street | TELECOM HOUSE MILLENIUM BUSINESS PARK |
| Manufacturer City | STEETON, WEST YORKSHIRE BD206RB |
| Manufacturer Country | UK |
| Manufacturer Postal | BD20 6RB |
| Manufacturer Phone | 053291000 |
| Single Use | 3 |
| Remedial Action | RL |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ACORN STAIRLIFT |
| Generic Name | STAIRWAY CHAIRLIFT |
| Product Code | PCD |
| Date Received | 2016-04-20 |
| Returned To Mfg | 2016-02-27 |
| Model Number | 180 |
| Operator | LAY USER/PATIENT |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ACORN MOBILITY SERVICES LTD |
| Manufacturer Address | TELECOM HOUSE MILLENIUM BUSINESS PARK STEETON, WEST YORKSHIRE BD206RB UK BD20 6RB |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2016-04-20 |